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rs122445107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122445107(C;G)
Make rs122445107(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77697589
GeneATRX
is asnp
is mentioned by
dbSNPrs122445107
ebirs122445107
HLIrs122445107
Exacrs122445107
Varsomers122445107
Maprs122445107
PheGenIrs122445107
hapmaprs122445107
1000 genomesrs122445107
hgdprs122445107
ensemblrs122445107
gopubmedrs122445107
geneviewrs122445107
scholarrs122445107
googlers122445107
pharmgkbrs122445107
gwascentralrs122445107
openSNPrs122445107
23andMers122445107
23andMe allrs122445107
SNP Nexus

SNPshotrs122445107
SNPdbers122445107
MSV3drs122445107
GWAS Ctlgrs122445107
Max Magnitude0
OMIM300032
Desc
Variant0021
Relatedalso
ClinVar
Risk rs122445107(G;G)
Alt rs122445107(G;G)
Reference rs122445107(C;C)
Significance Pathogenic
Disease Acquired hemoglobin H disease
Variation info
Gene ATRX
CLNDBN Acquired hemoglobin H disease
Reversed 1
HGVS NC_000023.10:g.76953077G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012507.4,