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rs778820577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778820577(C;T)
Make rs778820577(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63945392
GeneSCN4A
is asnp
is mentioned by
dbSNPrs778820577
dbSNP (classic)rs778820577
ClinGenrs778820577
ebirs778820577
HLIrs778820577
Exacrs778820577
Gnomadrs778820577
Varsomers778820577
LitVarrs778820577
Maprs778820577
PheGenIrs778820577
Biobankrs778820577
1000 genomesrs778820577
hgdprs778820577
ensemblrs778820577
geneviewrs778820577
scholarrs778820577
googlers778820577
pharmgkbrs778820577
gwascentralrs778820577
openSNPrs778820577
23andMers778820577
23andMe allrs778820577
SNPshotrs778820577
SNPdbers778820577
MSV3drs778820577
GWAS Ctlgrs778820577
Max Magnitude0
ClinVar
Risk rs778820577(T;T)
Alt rs778820577(T;T)
Reference Rs778820577(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.62022752C>T
CLNSRC
CLNACC RCV000418825.1,