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rs1057521988

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521988(C;C)
Make rs1057521988(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71118847
GeneMED12
is asnp
is mentioned by
dbSNPrs1057521988
dbSNP (old)rs1057521988
ClinGenrs1057521988
ebirs1057521988
HLIrs1057521988
Exacrs1057521988
Gnomadrs1057521988
Varsomers1057521988
Maprs1057521988
PheGenIrs1057521988
Biobankrs1057521988
1000 genomesrs1057521988
hgdprs1057521988
ensemblrs1057521988
gopubmedrs1057521988
geneviewrs1057521988
scholarrs1057521988
googlers1057521988
pharmgkbrs1057521988
gwascentralrs1057521988
openSNPrs1057521988
23andMers1057521988
23andMe allrs1057521988
SNPshotrs1057521988
SNPdbers1057521988
MSV3drs1057521988
GWAS Ctlgrs1057521988
Max Magnitude0
ClinVar
Risk rs1057521988(C;C)
Alt rs1057521988(C;C)
Reference Rs1057521988(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70338697G>C
CLNSRC
CLNACC RCV000433847.1,