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rs796053105

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053105(-;-)
Make rs796053105(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051741
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053105
ebirs796053105
HLIrs796053105
Exacrs796053105
Varsomers796053105
Maprs796053105
PheGenIrs796053105
hapmaprs796053105
1000 genomesrs796053105
hgdprs796053105
ensemblrs796053105
gopubmedrs796053105
geneviewrs796053105
scholarrs796053105
googlers796053105
pharmgkbrs796053105
gwascentralrs796053105
openSNPrs796053105
23andMers796053105
23andMe allrs796053105
SNP Nexus

SNPshotrs796053105
SNPdbers796053105
MSV3drs796053105
GWAS Ctlgrs796053105
Max Magnitude0
ClinVar
Risk rs796053105(;)
Alt rs796053105(;)
Reference rs796053105(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908251delC
CLNSRC
CLNACC RCV000189097.1,