Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs750612085
rs750612085
1.000 15 77615044 missense variant T/C snv 1.2E-05
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
0.800 1.000 1 2018 2018
dbSNP: rs757077698
rs757077698
1.000 15 77615038 missense variant C/T snv 2.8E-05
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64
0.800 1.000 1 2018 2018
dbSNP: rs11855853
rs11855853
15 77720276 intron variant C/T snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs11856579
rs11856579
15 77720346 intron variant G/A snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs3935685
rs3935685
15 77741926 intron variant T/C snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4468571
rs4468571
1.000 0.040 15 77727790 intron variant A/G snv 0.35
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs4468571
rs4468571
1.000 0.040 15 77727790 intron variant A/G snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs62007820
rs62007820
15 77768444 intron variant G/A snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019