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rs1064795423

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position101176363
GeneNALCN
is asnp
is mentioned by
dbSNPrs1064795423
dbSNP (old)rs1064795423
ClinGenrs1064795423
ebirs1064795423
HLIrs1064795423
Exacrs1064795423
Gnomadrs1064795423
Varsomers1064795423
Maprs1064795423
PheGenIrs1064795423
Biobankrs1064795423
1000 genomesrs1064795423
hgdprs1064795423
ensemblrs1064795423
gopubmedrs1064795423
geneviewrs1064795423
scholarrs1064795423
googlers1064795423
pharmgkbrs1064795423
gwascentralrs1064795423
openSNPrs1064795423
23andMers1064795423
23andMe allrs1064795423
SNPshotrs1064795423
SNPdbers1064795423
MSV3drs1064795423
GWAS Ctlgrs1064795423
Max Magnitude0
ClinVar
Risk rs1064795423(G;G)
Alt rs1064795423(G;G)
Reference Rs1064795423(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NALCN
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.101828714A>C
CLNSRC
CLNACC RCV000486031.1,