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

rs122445098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs122445098(A;G)
Make rs122445098(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77558685
GeneATRX
is asnp
is mentioned by
dbSNPrs122445098
ebirs122445098
HLIrs122445098
Exacrs122445098
Varsomers122445098
Maprs122445098
PheGenIrs122445098
hapmaprs122445098
1000 genomesrs122445098
hgdprs122445098
ensemblrs122445098
gopubmedrs122445098
geneviewrs122445098
scholarrs122445098
googlers122445098
pharmgkbrs122445098
gwascentralrs122445098
openSNPrs122445098
23andMers122445098
23andMe allrs122445098
SNP Nexus

SNPshotrs122445098
SNPdbers122445098
MSV3drs122445098
GWAS Ctlgrs122445098
Max Magnitude0
OMIM300032
Desc
Variant0007
Relatedalso
ClinVar
Risk rs122445098(G;G)
Alt rs122445098(G;G)
Reference rs122445098(A;A)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76814156T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012493.16,