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rs797044985

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044985(G;G)
Make rs797044985(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166037774
GeneSCN1A
is asnp
is mentioned by
dbSNPrs797044985
ebirs797044985
HLIrs797044985
Exacrs797044985
Varsomers797044985
Maprs797044985
PheGenIrs797044985
hapmaprs797044985
1000 genomesrs797044985
hgdprs797044985
ensemblrs797044985
gopubmedrs797044985
geneviewrs797044985
scholarrs797044985
googlers797044985
pharmgkbrs797044985
gwascentralrs797044985
openSNPrs797044985
23andMers797044985
23andMe allrs797044985
SNP Nexus

SNPshotrs797044985
SNPdbers797044985
MSV3drs797044985
GWAS Ctlgrs797044985
Max Magnitude0
ClinVar
Risk rs797044985(G;G)
Alt rs797044985(G;G)
Reference rs797044985(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894284A>C
CLNSRC
CLNACC RCV000190449.1,