Source: CLINVAR ×
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: rs1562005199
rs1562005199
1 6 69382853 missense variant G/A snv 0.700 0
dbSNP: rs1562137453
rs1562137453
1 6 69049307 missense variant T/C snv 0.700 0