Have questions? Visit https://www.reddit.com/r/SNPedia

rs122445097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122445097(C;C)
Make rs122445097(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77574326
GeneATRX
is asnp
is mentioned by
dbSNPrs122445097
ebirs122445097
HLIrs122445097
Exacrs122445097
Varsomers122445097
Maprs122445097
PheGenIrs122445097
hapmaprs122445097
1000 genomesrs122445097
hgdprs122445097
ensemblrs122445097
gopubmedrs122445097
geneviewrs122445097
scholarrs122445097
googlers122445097
pharmgkbrs122445097
gwascentralrs122445097
openSNPrs122445097
23andMers122445097
23andMe allrs122445097
SNP Nexus

SNPshotrs122445097
SNPdbers122445097
MSV3drs122445097
GWAS Ctlgrs122445097
Max Magnitude0
OMIM300032
Desc
Variant0006
Relatedalso
ClinVar
Risk rs122445097(C;C)
Alt rs122445097(C;C)
Reference rs122445097(T;T)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76829791A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012492.14,