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rs797044865

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044865(A;G)
Make rs797044865(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position77684516
GeneATRX
is asnp
is mentioned by
dbSNPrs797044865
ebirs797044865
HLIrs797044865
Exacrs797044865
Varsomers797044865
Maprs797044865
PheGenIrs797044865
hapmaprs797044865
1000 genomesrs797044865
hgdprs797044865
ensemblrs797044865
gopubmedrs797044865
geneviewrs797044865
scholarrs797044865
googlers797044865
pharmgkbrs797044865
gwascentralrs797044865
openSNPrs797044865
23andMers797044865
23andMe allrs797044865
SNP Nexus

SNPshotrs797044865
SNPdbers797044865
MSV3drs797044865
GWAS Ctlgrs797044865
Max Magnitude0
ClinVar
Risk rs797044865(G;G)
Alt rs797044865(G;G)
Reference rs797044865(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ATRX
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.76940008T>C
CLNSRC
CLNACC RCV000190670.1,