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rs972964381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs972964381(C;C)
Make rs972964381(C;T)
Make rs972964381(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position101143190
GeneNALCN
is asnp
is mentioned by
dbSNPrs972964381
dbSNP (classic)rs972964381
ClinGenrs972964381
ebirs972964381
HLIrs972964381
Exacrs972964381
Gnomadrs972964381
Varsomers972964381
LitVarrs972964381
Maprs972964381
PheGenIrs972964381
Biobankrs972964381
1000 genomesrs972964381
hgdprs972964381
ensemblrs972964381
geneviewrs972964381
scholarrs972964381
googlers972964381
pharmgkbrs972964381
gwascentralrs972964381
openSNPrs972964381
23andMers972964381
23andMe allrs972964381
SNPshotrs972964381
SNPdbers972964381
MSV3drs972964381
GWAS Ctlgrs972964381
Max Magnitude0
ClinVar
Risk rs972964381(A;A)
Alt rs972964381(A;A)
Reference Rs972964381(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NALCN
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.101795541G>A
CLNSRC
CLNACC RCV000423757.1,