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

rs869312952

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312952(A;A)
Make rs869312952(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position101073583
GeneNALCN
is asnp
is mentioned by
dbSNPrs869312952
ebirs869312952
HLIrs869312952
Exacrs869312952
Varsomers869312952
Maprs869312952
PheGenIrs869312952
hapmaprs869312952
1000 genomesrs869312952
hgdprs869312952
ensemblrs869312952
gopubmedrs869312952
geneviewrs869312952
scholarrs869312952
googlers869312952
pharmgkbrs869312952
gwascentralrs869312952
openSNPrs869312952
23andMers869312952
23andMe allrs869312952
SNP Nexus

SNPshotrs869312952
SNPdbers869312952
MSV3drs869312952
GWAS Ctlgrs869312952
Max Magnitude0
ClinVar
Risk rs869312952(A;A)
Alt rs869312952(A;A)
Reference rs869312952(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NALCN
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000013.10:g.101725935C>T
CLNSRC
CLNACC RCV000210682.1,