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rs122445095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122445095(G;T)
Make rs122445095(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77633572
GeneATRX
is asnp
is mentioned by
dbSNPrs122445095
ebirs122445095
HLIrs122445095
Exacrs122445095
Varsomers122445095
Maprs122445095
PheGenIrs122445095
hapmaprs122445095
1000 genomesrs122445095
hgdprs122445095
ensemblrs122445095
gopubmedrs122445095
geneviewrs122445095
scholarrs122445095
googlers122445095
pharmgkbrs122445095
gwascentralrs122445095
openSNPrs122445095
23andMers122445095
23andMe allrs122445095
SNP Nexus

SNPshotrs122445095
SNPdbers122445095
MSV3drs122445095
GWAS Ctlgrs122445095
Max Magnitude0
OMIM300032
Desc
Variant0003
Relatedalso
ClinVar
Risk rs122445095(A,T;A,T)
Alt rs122445095(A,T;A,T)
Reference rs122445095(G;G)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76889060C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012489.22,