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: rs768737101
rs768737101
DCHS1
1 1.000 0.040 11 6625356 missense variant G/A snv 2.4E-05 3.5E-05 0.800 1.000 1 2015 2015
dbSNP: rs201457110
rs201457110
DCHS1
1 1.000 0.040 11 6624138 missense variant C/T snv 4.2E-04 1.4E-04 0.700 1.000 1 2015 2015