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rs398124611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124611(A;A)
Make rs398124611(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position17721541
GeneNHS
is asnp
is mentioned by
dbSNPrs398124611
ebirs398124611
HLIrs398124611
Exacrs398124611
Varsomers398124611
Maprs398124611
PheGenIrs398124611
hapmaprs398124611
1000 genomesrs398124611
hgdprs398124611
ensemblrs398124611
gopubmedrs398124611
geneviewrs398124611
scholarrs398124611
googlers398124611
pharmgkbrs398124611
gwascentralrs398124611
openSNPrs398124611
23andMers398124611
23andMe allrs398124611
SNP Nexus

SNPshotrs398124611
SNPdbers398124611
MSV3drs398124611
GWAS Ctlgrs398124611
Max Magnitude0
ClinVar
Risk rs398124611(A;A)
Alt rs398124611(A;A)
Reference rs398124611(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NHS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.17739661G>A
CLNSRC ClinVar Emory University
CLNACC RCV000082808.4,