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rs1057524290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524290(C;C)
Make rs1057524290(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63959273
GeneLOC105371858, SCN4A
is asnp
is mentioned by
dbSNPrs1057524290
dbSNP (classic)rs1057524290
ClinGenrs1057524290
ebirs1057524290
HLIrs1057524290
Exacrs1057524290
Gnomadrs1057524290
Varsomers1057524290
LitVarrs1057524290
Maprs1057524290
PheGenIrs1057524290
Biobankrs1057524290
1000 genomesrs1057524290
hgdprs1057524290
ensemblrs1057524290
geneviewrs1057524290
scholarrs1057524290
googlers1057524290
pharmgkbrs1057524290
gwascentralrs1057524290
openSNPrs1057524290
23andMers1057524290
SNPshotrs1057524290
SNPdbers1057524290
MSV3drs1057524290
GWAS Ctlgrs1057524290
Max Magnitude0
ClinVar
Risk rs1057524290(C;C)
Alt rs1057524290(C;C)
Reference Rs1057524290(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.62036633A>G
CLNSRC
CLNACC RCV000440430.1,