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rs137852222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852222(G;G)
Make rs137852222(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77841311
GeneMAGT1
is asnp
is mentioned by
dbSNPrs137852222
ebirs137852222
HLIrs137852222
Exacrs137852222
Varsomers137852222
Maprs137852222
PheGenIrs137852222
hapmaprs137852222
1000 genomesrs137852222
hgdprs137852222
ensemblrs137852222
gopubmedrs137852222
geneviewrs137852222
scholarrs137852222
googlers137852222
pharmgkbrs137852222
gwascentralrs137852222
openSNPrs137852222
23andMers137852222
23andMe allrs137852222
SNP Nexus

SNPshotrs137852222
SNPdbers137852222
MSV3drs137852222
GWAS Ctlgrs137852222
Max Magnitude0
OMIM300715
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852222(G;G)
Alt rs137852222(G;G)
Reference rs137852222(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MAGT1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.77096808A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000088658.2,