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rs1057521065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521065(C;C)
Make rs1057521065(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63968310
GeneSCN4A
is asnp
is mentioned by
dbSNPrs1057521065
dbSNP (old)rs1057521065
ClinGenrs1057521065
ebirs1057521065
HLIrs1057521065
Exacrs1057521065
Gnomadrs1057521065
Varsomers1057521065
Maprs1057521065
PheGenIrs1057521065
Biobankrs1057521065
1000 genomesrs1057521065
hgdprs1057521065
ensemblrs1057521065
gopubmedrs1057521065
geneviewrs1057521065
scholarrs1057521065
googlers1057521065
pharmgkbrs1057521065
gwascentralrs1057521065
openSNPrs1057521065
23andMers1057521065
23andMe allrs1057521065
SNPshotrs1057521065
SNPdbers1057521065
MSV3drs1057521065
GWAS Ctlgrs1057521065
Max Magnitude0
ClinVar
Risk rs1057521065(C;C)
Alt rs1057521065(C;C)
Reference Rs1057521065(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.62045670A>G
CLNSRC
CLNACC RCV000439261.1,