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rs1064794722

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position101192008
GeneNALCN
is asnp
is mentioned by
dbSNPrs1064794722
dbSNP (old)rs1064794722
ClinGenrs1064794722
ebirs1064794722
HLIrs1064794722
Exacrs1064794722
Gnomadrs1064794722
Varsomers1064794722
Maprs1064794722
PheGenIrs1064794722
Biobankrs1064794722
1000 genomesrs1064794722
hgdprs1064794722
ensemblrs1064794722
gopubmedrs1064794722
geneviewrs1064794722
scholarrs1064794722
googlers1064794722
pharmgkbrs1064794722
gwascentralrs1064794722
openSNPrs1064794722
23andMers1064794722
23andMe allrs1064794722
SNPshotrs1064794722
SNPdbers1064794722
MSV3drs1064794722
GWAS Ctlgrs1064794722
Max Magnitude0
ClinVar
Risk rs1064794722(G;G)
Alt rs1064794722(G;G)
Reference Rs1064794722(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NALCN
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.101844359T>C
CLNSRC
CLNACC RCV000483143.1,