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rs122445105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122445105(C;T)
Make rs122445105(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77684520
GeneATRX
is asnp
is mentioned by
dbSNPrs122445105
ebirs122445105
HLIrs122445105
Exacrs122445105
Varsomers122445105
Maprs122445105
PheGenIrs122445105
hapmaprs122445105
1000 genomesrs122445105
hgdprs122445105
ensemblrs122445105
gopubmedrs122445105
geneviewrs122445105
scholarrs122445105
googlers122445105
pharmgkbrs122445105
gwascentralrs122445105
openSNPrs122445105
23andMers122445105
23andMe allrs122445105
SNP Nexus

SNPshotrs122445105
SNPdbers122445105
MSV3drs122445105
GWAS Ctlgrs122445105
Max Magnitude0
OMIM300032
Desc
Variant0018
Relatedalso
ClinVar
Risk rs122445105(T;T)
Alt rs122445105(T;T)
Reference rs122445105(C;C)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene ATRX
CLNDBN not provided Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.76940012G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000078972.4, RCV000190796.1,