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

rs122445104

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs122445104(A;A)
Make rs122445104(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77620442
GeneATRX
is asnp
is mentioned by
dbSNPrs122445104
ebirs122445104
HLIrs122445104
Exacrs122445104
Varsomers122445104
Maprs122445104
PheGenIrs122445104
hapmaprs122445104
1000 genomesrs122445104
hgdprs122445104
ensemblrs122445104
gopubmedrs122445104
geneviewrs122445104
scholarrs122445104
googlers122445104
pharmgkbrs122445104
gwascentralrs122445104
openSNPrs122445104
23andMers122445104
23andMe allrs122445104
SNP Nexus

SNPshotrs122445104
SNPdbers122445104
MSV3drs122445104
GWAS Ctlgrs122445104
Max Magnitude0
OMIM300032
Desc
Variant0016
Relatedalso
ClinVar
Risk rs122445104(A;A)
Alt rs122445104(A;A)
Reference rs122445104(G;G)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76875910C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012502.16,