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rs587776756

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776756(C;T)
Make rs587776756(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position77785981
GeneATRX
is asnp
is mentioned by
dbSNPrs587776756
ClinGenrs587776756
ebirs587776756
HLIrs587776756
Exacrs587776756
Varsomers587776756
Maprs587776756
PheGenIrs587776756
hapmaprs587776756
1000 genomesrs587776756
hgdprs587776756
ensemblrs587776756
gopubmedrs587776756
geneviewrs587776756
scholarrs587776756
googlers587776756
pharmgkbrs587776756
gwascentralrs587776756
openSNPrs587776756
23andMers587776756
23andMe allrs587776756
SNP Nexus

SNPshotrs587776756
SNPdbers587776756
MSV3drs587776756
GWAS Ctlgrs587776756
Max Magnitude0
ClinVar
Risk Rs587776756(C;C) rs587776756(T;T)
Alt Rs587776756(C;C) rs587776756(T;T)
Reference Rs587776756(G;G)
Significance Pathogenic
Disease Acquired hemoglobin H disease
Variation info
Gene ATRX
CLNDBN Acquired hemoglobin H disease
Reversed 1
HGVS NC_000023.10:g.77041467C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012506.4,