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rs122445094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122445094(C;C)
Make rs122445094(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77633682
GeneATRX
is asnp
is mentioned by
dbSNPrs122445094
ebirs122445094
HLIrs122445094
Exacrs122445094
Varsomers122445094
Maprs122445094
PheGenIrs122445094
hapmaprs122445094
1000 genomesrs122445094
hgdprs122445094
ensemblrs122445094
gopubmedrs122445094
geneviewrs122445094
scholarrs122445094
googlers122445094
pharmgkbrs122445094
gwascentralrs122445094
openSNPrs122445094
23andMers122445094
23andMe allrs122445094
SNP Nexus

SNPshotrs122445094
SNPdbers122445094
MSV3drs122445094
GWAS Ctlgrs122445094
Max Magnitude0
OMIM300032
Desc
Variant0002
Relatedalso
ClinVar
Risk rs122445094(C;C)
Alt rs122445094(C;C)
Reference rs122445094(T;T)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76889170A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012488.24,