Have questions? Visit https://www.reddit.com/r/SNPedia

rs372969054

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372969054(A;A)
Make rs372969054(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position17724365
GeneNHS
is asnp
is mentioned by
dbSNPrs372969054
ebirs372969054
HLIrs372969054
Exacrs372969054
Varsomers372969054
Maprs372969054
PheGenIrs372969054
hapmaprs372969054
1000 genomesrs372969054
hgdprs372969054
ensemblrs372969054
gopubmedrs372969054
geneviewrs372969054
scholarrs372969054
googlers372969054
pharmgkbrs372969054
gwascentralrs372969054
openSNPrs372969054
23andMers372969054
23andMe allrs372969054
SNP Nexus

SNPshotrs372969054
SNPdbers372969054
MSV3drs372969054
GWAS Ctlgrs372969054
Max Magnitude0
ClinVar
Risk rs372969054(A;A)
Alt rs372969054(A;A)
Reference rs372969054(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NHS
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.17742485G>A
CLNSRC
CLNACC RCV000190792.1,