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rs121918362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918362(G;T)
Make rs121918362(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position46501237
GeneZNF674
is asnp
is mentioned by
dbSNPrs121918362
ebirs121918362
HLIrs121918362
Exacrs121918362
Varsomers121918362
Maprs121918362
PheGenIrs121918362
hapmaprs121918362
1000 genomesrs121918362
hgdprs121918362
ensemblrs121918362
gopubmedrs121918362
geneviewrs121918362
scholarrs121918362
googlers121918362
pharmgkbrs121918362
gwascentralrs121918362
openSNPrs121918362
23andMers121918362
23andMe allrs121918362
SNP Nexus

SNPshotrs121918362
SNPdbers121918362
MSV3drs121918362
GWAS Ctlgrs121918362
Max Magnitude0
OMIM300573
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918362(T;T)
Alt rs121918362(T;T)
Reference rs121918362(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ZNF674
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.46360672C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000088657.2,