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rs104894953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894953(A;A)
Make rs104894953(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position37728068
GeneXK
is asnp
is mentioned by
dbSNPrs104894953
ebirs104894953
HLIrs104894953
Exacrs104894953
Varsomers104894953
Maprs104894953
PheGenIrs104894953
hapmaprs104894953
1000 genomesrs104894953
hgdprs104894953
ensemblrs104894953
gopubmedrs104894953
geneviewrs104894953
scholarrs104894953
googlers104894953
pharmgkbrs104894953
gwascentralrs104894953
openSNPrs104894953
23andMers104894953
23andMe allrs104894953
SNP Nexus

SNPshotrs104894953
SNPdbers104894953
MSV3drs104894953
GWAS Ctlgrs104894953
Max Magnitude0
OMIM314850
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104894953(A;A)
Alt rs104894953(A;A)
Reference rs104894953(G;G)
Significance Pathogenic
Disease McLeod neuroacanthocytosis syndrome
Variation info
Gene XK
CLNDBN McLeod neuroacanthocytosis syndrome
Reversed 0
HGVS NC_000023.10:g.37587321G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010424.4,