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: rs267607048
rs267607048
SHOC2
16 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 0.050 1.000 5 2009 2015
dbSNP: rs1441638629
rs1441638629
CSHL1 ; GH1
2 0.925 0.200 17 63918773 missense variant C/T snv 4.0E-06 1.4E-05 0.030 1.000 3 2012 2015
dbSNP: rs745410279
rs745410279
IGF1
2 0.925 0.200 12 102478498 missense variant T/C snv 4.1E-06 0.030 1.000 3 2012 2015
dbSNP: rs113461014
rs113461014
STAT5B
2 0.925 0.200 17 42232124 missense variant C/T snv 0.010 1.000 1 2012 2012