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rs45439799

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45439799(A;G)
Make rs45439799(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77600552
GeneATRX
is asnp
is mentioned by
dbSNPrs45439799
ebirs45439799
HLIrs45439799
Exacrs45439799
Varsomers45439799
Maprs45439799
PheGenIrs45439799
hapmaprs45439799
1000 genomesrs45439799
hgdprs45439799
ensemblrs45439799
gopubmedrs45439799
geneviewrs45439799
scholarrs45439799
googlers45439799
pharmgkbrs45439799
gwascentralrs45439799
openSNPrs45439799
23andMers45439799
23andMe allrs45439799
SNP Nexus

SNPshotrs45439799
SNPdbers45439799
MSV3drs45439799
GWAS Ctlgrs45439799
GMAF0.003628
Max Magnitude0
OMIM300032
Desc
Variant0004
Relatedalso
ClinVar
Risk rs45439799(C,G;C,G)
Alt rs45439799(C,G;C,G)
Reference rs45439799(A;A)
Significance Pathogenic
Disease ATR-X syndrome not specified
Variation info
Gene ATRX
CLNDBN ATR-X syndrome not specified
Reversed 1
HGVS NC_000023.10:g.76856021T>C
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012490.16, RCV000078966.6,