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rs122445106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122445106(C;T)
Make rs122445106(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77633660
GeneATRX
is asnp
is mentioned by
dbSNPrs122445106
ebirs122445106
HLIrs122445106
Exacrs122445106
Varsomers122445106
Maprs122445106
PheGenIrs122445106
hapmaprs122445106
1000 genomesrs122445106
hgdprs122445106
ensemblrs122445106
gopubmedrs122445106
geneviewrs122445106
scholarrs122445106
googlers122445106
pharmgkbrs122445106
gwascentralrs122445106
openSNPrs122445106
23andMers122445106
23andMe allrs122445106
SNP Nexus

SNPshotrs122445106
SNPdbers122445106
MSV3drs122445106
GWAS Ctlgrs122445106
Max Magnitude0
OMIM300032
Desc
Variant0019
Relatedalso
ClinVar
Risk rs122445106(T;T)
Alt rs122445106(T;T)
Reference rs122445106(C;C)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76889148G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012505.24,