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rs1085307941

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position71141950
GeneMED12
is asnp
is mentioned by
dbSNPrs1085307941
dbSNP (old)rs1085307941
ClinGenrs1085307941
ebirs1085307941
HLIrs1085307941
Exacrs1085307941
Gnomadrs1085307941
Varsomers1085307941
Maprs1085307941
PheGenIrs1085307941
Biobankrs1085307941
1000 genomesrs1085307941
hgdprs1085307941
ensemblrs1085307941
gopubmedrs1085307941
geneviewrs1085307941
scholarrs1085307941
googlers1085307941
pharmgkbrs1085307941
gwascentralrs1085307941
openSNPrs1085307941
23andMers1085307941
23andMe allrs1085307941
SNPshotrs1085307941
SNPdbers1085307941
MSV3drs1085307941
GWAS Ctlgrs1085307941
Max Magnitude0
ClinVar
Risk rs1085307941(C;C)
Alt rs1085307941(C;C)
Reference Rs1085307941(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70361800A>C
CLNSRC
CLNACC RCV000488923.1,