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rs122445096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs122445096(A;T)
Make rs122445096(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77593702
GeneATRX
is asnp
is mentioned by
dbSNPrs122445096
ebirs122445096
HLIrs122445096
Exacrs122445096
Varsomers122445096
Maprs122445096
PheGenIrs122445096
hapmaprs122445096
1000 genomesrs122445096
hgdprs122445096
ensemblrs122445096
gopubmedrs122445096
geneviewrs122445096
scholarrs122445096
googlers122445096
pharmgkbrs122445096
gwascentralrs122445096
openSNPrs122445096
23andMers122445096
23andMe allrs122445096
SNP Nexus

SNPshotrs122445096
SNPdbers122445096
MSV3drs122445096
GWAS Ctlgrs122445096
Max Magnitude0
OMIM300032
Desc
Variant0005
Relatedalso
ClinVar
Risk rs122445096(T;T)
Alt rs122445096(T;T)
Reference rs122445096(A;A)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76849172T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012491.14,