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rs398124608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124608(-;-)
Make rs398124608(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position17376157
GeneNHS
is asnp
is mentioned by
dbSNPrs398124608
ebirs398124608
HLIrs398124608
Exacrs398124608
Varsomers398124608
Maprs398124608
PheGenIrs398124608
hapmaprs398124608
1000 genomesrs398124608
hgdprs398124608
ensemblrs398124608
gopubmedrs398124608
geneviewrs398124608
scholarrs398124608
googlers398124608
pharmgkbrs398124608
gwascentralrs398124608
openSNPrs398124608
23andMers398124608
23andMe allrs398124608
SNP Nexus

SNPshotrs398124608
SNPdbers398124608
MSV3drs398124608
GWAS Ctlgrs398124608
Max Magnitude0
ClinVar
Risk rs398124608(;)
Alt rs398124608(;)
Reference rs398124608(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NHS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.17394280delC
CLNSRC HGMD
CLNACC RCV000082803.4,