Gene: VWC2L ×
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: rs17711053
rs17711053
VWC2L
2 1.000 0.040 2 214574984 intron variant A/G snv 0.11 0.700 1.000 1 2018 2018