Source: CLINVAR

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: rs121913476
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv
CUI: C0279763
Disease: endometrial adenoacanthoma
endometrial adenoacanthoma 		0.700 1.000 4 2008 2013
dbSNP: rs121913476
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs121913476
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs121913476
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs121913476
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 1 2016 2016