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rs757674263

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757674263(A;A)
Make rs757674263(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position101111216
GeneNALCN
is asnp
is mentioned by
dbSNPrs757674263
ebirs757674263
HLIrs757674263
Exacrs757674263
Varsomers757674263
Maprs757674263
PheGenIrs757674263
hapmaprs757674263
1000 genomesrs757674263
hgdprs757674263
ensemblrs757674263
gopubmedrs757674263
geneviewrs757674263
scholarrs757674263
googlers757674263
pharmgkbrs757674263
gwascentralrs757674263
openSNPrs757674263
23andMers757674263
23andMe allrs757674263
SNP Nexus

SNPshotrs757674263
SNPdbers757674263
MSV3drs757674263
GWAS Ctlgrs757674263
Max Magnitude0
ClinVar
Risk rs757674263(A;A)
Alt rs757674263(A;A)
Reference rs757674263(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NALCN
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000013.10:g.101763567G>A
CLNSRC
CLNACC RCV000210615.1,