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rs1064796154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome13
Position101061970
GeneNALCN
is asnp
is mentioned by
dbSNPrs1064796154
dbSNP (old)rs1064796154
ClinGenrs1064796154
ebirs1064796154
HLIrs1064796154
Exacrs1064796154
Gnomadrs1064796154
Varsomers1064796154
LitVarrs1064796154
Maprs1064796154
PheGenIrs1064796154
Biobankrs1064796154
1000 genomesrs1064796154
hgdprs1064796154
ensemblrs1064796154
gopubmedrs1064796154
geneviewrs1064796154
scholarrs1064796154
googlers1064796154
pharmgkbrs1064796154
gwascentralrs1064796154
openSNPrs1064796154
23andMers1064796154
23andMe allrs1064796154
SNPshotrs1064796154
SNPdbers1064796154
MSV3drs1064796154
GWAS Ctlgrs1064796154
Max Magnitude0
ClinVar
Risk rs1064796154(-;-)
Alt rs1064796154(-;-)
Reference Rs1064796154(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene NALCN
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.101714322_101714323delCT
CLNSRC
CLNACC RCV000481215.1,