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rs122445099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122445099(C;T)
Make rs122445099(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77520832
GeneATRX
is asnp
is mentioned by
dbSNPrs122445099
ebirs122445099
HLIrs122445099
Exacrs122445099
Varsomers122445099
Maprs122445099
PheGenIrs122445099
hapmaprs122445099
1000 genomesrs122445099
hgdprs122445099
ensemblrs122445099
gopubmedrs122445099
geneviewrs122445099
scholarrs122445099
googlers122445099
pharmgkbrs122445099
gwascentralrs122445099
openSNPrs122445099
23andMers122445099
23andMe allrs122445099
SNP Nexus

SNPshotrs122445099
SNPdbers122445099
MSV3drs122445099
GWAS Ctlgrs122445099
Max Magnitude0
OMIM300032
Desc
Variant0008
Relatedalso
ClinVar
Risk rs122445099(T;T)
Alt rs122445099(T;T)
Reference rs122445099(C;C)
Significance Pathogenic
Disease ATR-X syndrome
Variation info
Gene ATRX
CLNDBN ATR-X syndrome
Reversed 1
HGVS NC_000023.10:g.76776310G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012494.22,