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rs1057520846

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520846(C;C)
Make rs1057520846(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63941819
GeneSCN4A
is asnp
is mentioned by
dbSNPrs1057520846
dbSNP (old)rs1057520846
ClinGenrs1057520846
ebirs1057520846
HLIrs1057520846
Exacrs1057520846
Gnomadrs1057520846
Varsomers1057520846
Maprs1057520846
PheGenIrs1057520846
Biobankrs1057520846
1000 genomesrs1057520846
hgdprs1057520846
ensemblrs1057520846
gopubmedrs1057520846
geneviewrs1057520846
scholarrs1057520846
googlers1057520846
pharmgkbrs1057520846
gwascentralrs1057520846
openSNPrs1057520846
23andMers1057520846
23andMe allrs1057520846
SNPshotrs1057520846
SNPdbers1057520846
MSV3drs1057520846
GWAS Ctlgrs1057520846
Max Magnitude0
ClinVar
Risk rs1057520846(C;C)
Alt rs1057520846(C;C)
Reference Rs1057520846(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.62019179A>G
CLNSRC
CLNACC RCV000427535.1,