Gene: WNT3 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs199501
rs199501
WNT3 ; LRRC37A2
1 17 46785247 intron variant A/G snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs199505
rs199505
WNT3 ; LRRC37A2
4 0.925 0.120 17 46782044 intron variant A/G snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs199506
rs199506
WNT3 ; LRRC37A2
1 17 46781665 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs199507
rs199507
WNT3 ; LRRC37A2
1 17 46781489 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs199509
rs199509
WNT3 ; LRRC37A2
1 17 46781362 intron variant G/A snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs199514
rs199514
WNT3 ; LRRC37A2
2 1.000 0.080 17 46779515 intron variant G/A snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs199515
rs199515
WNT3 ; LRRC37A2
3 0.925 0.120 17 46779275 intron variant G/C snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs199520
rs199520
WNT3 ; LRRC37A2
1 17 46776506 intron variant G/A snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs199528
rs199528
WNT3 ; LRRC37A2
1 17 46765770 intron variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs2074404
rs2074404
WNT3 ; LRRC37A2
4 0.925 0.120 17 46788073 intron variant T/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs415430
rs415430
WNT3 ; LRRC37A2
3 1.000 0.040 17 46781778 intron variant C/T snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs70602
rs70602
WNT3 ; LRRC37A2
2 1.000 0.080 17 46782349 intron variant T/C snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs916888
rs916888
WNT3 ; LRRC37A2
4 17 46785767 intron variant T/C snv 0.19 0.700 1.000 1 2012 2012