Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1440530084
rs1440530084
0.882 0.040 17 42563227 missense variant G/A snv 4.0E-06 1.4E-05
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia
0.030 1.000 3 2013 2017
dbSNP: rs761347168
rs761347168
1.000 17 42563226 missense variant C/T snv 8.0E-06
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia
0.030 1.000 3 2013 2017
dbSNP: rs1440530084
rs1440530084
0.882 0.040 17 42563227 missense variant G/A snv 4.0E-06 1.4E-05
CUI: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
0.020 1.000 2 2017 2017
dbSNP: rs1440530084
rs1440530084
0.882 0.040 17 42563227 missense variant G/A snv 4.0E-06 1.4E-05
CUI: C0242292
Disease: McCune-Albright Syndrome
McCune-Albright Syndrome
0.010 1.000 1 2017 2017
dbSNP: rs148652390
rs148652390
1.000 0.080 17 42564085 synonymous variant C/A;G;T snv 1.7E-04; 1.6E-03
Diabetes Mellitus, Non-Insulin-Dependent
0.010 < 0.001 1 2017 2017
dbSNP: rs598126
rs598126
0.925 0.080 17 42564502 synonymous variant A/G snv 0.53 0.50
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2011 2011
dbSNP: rs598126
rs598126
0.925 0.080 17 42564502 synonymous variant A/G snv 0.53 0.50
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs746673818
rs746673818
17 42562625 start lost G/A snv
CUI: C0030552
Disease: Paresis
Paresis
0.010 1.000 1 2017 2017
dbSNP: rs746673818
rs746673818
17 42562625 start lost G/A snv
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
0.010 1.000 1 2017 2017
dbSNP: rs764492939
rs764492939
17 42562414 start lost G/A snv 1.6E-05 2.1E-05
CUI: C0030552
Disease: Paresis
Paresis
0.010 1.000 1 2017 2017
dbSNP: rs764492939
rs764492939
17 42562414 start lost G/A snv 1.6E-05 2.1E-05
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness
0.010 1.000 1 2017 2017