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rs9513851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs9513851(A;A)
Make rs9513851(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position101095633
GeneNALCN
is asnp
is mentioned by
dbSNPrs9513851
ebirs9513851
HLIrs9513851
Exacrs9513851
Varsomers9513851
Maprs9513851
PheGenIrs9513851
hapmaprs9513851
1000 genomesrs9513851
hgdprs9513851
ensemblrs9513851
gopubmedrs9513851
geneviewrs9513851
scholarrs9513851
googlers9513851
pharmgkbrs9513851
gwascentralrs9513851
openSNPrs9513851
23andMers9513851
23andMe allrs9513851
SNP Nexus

SNPshotrs9513851
SNPdbers9513851
MSV3drs9513851
GWAS Ctlgrs9513851
GMAF0.04545
Max Magnitude0
? (A;A) (A;G) (G;G) 28


ClinVar
Risk rs9513851(A;A)
Alt rs9513851(A;A)
Reference Rs9513851(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene NALCN
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.101747984G>A
CLNSRC
CLNACC RCV000246356.1,