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rs796053058

From SNPedia

Orientationminus
Geno Mag Summary
(GAAAG;GAAAG) 0 common in clinvar
Make rs796053058(-;-)
Make rs796053058(-;GAAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166045183
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053058
ebirs796053058
HLIrs796053058
Exacrs796053058
Varsomers796053058
Maprs796053058
PheGenIrs796053058
hapmaprs796053058
1000 genomesrs796053058
hgdprs796053058
ensemblrs796053058
gopubmedrs796053058
geneviewrs796053058
scholarrs796053058
googlers796053058
pharmgkbrs796053058
gwascentralrs796053058
openSNPrs796053058
23andMers796053058
23andMe allrs796053058
SNP Nexus

SNPshotrs796053058
SNPdbers796053058
MSV3drs796053058
GWAS Ctlgrs796053058
Max Magnitude0
ClinVar
Risk rs796053058(;)
Alt rs796053058(;)
Reference rs796053058(GAAAG;GAAAG)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901693_166901697delCTTTC
CLNSRC
CLNACC RCV000189038.1,