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rs796053075

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053075(-;-)
Make rs796053075(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166073482
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053075
ebirs796053075
HLIrs796053075
Exacrs796053075
Varsomers796053075
Maprs796053075
PheGenIrs796053075
hapmaprs796053075
1000 genomesrs796053075
hgdprs796053075
ensemblrs796053075
gopubmedrs796053075
geneviewrs796053075
scholarrs796053075
googlers796053075
pharmgkbrs796053075
gwascentralrs796053075
openSNPrs796053075
23andMers796053075
23andMe allrs796053075
SNP Nexus

SNPshotrs796053075
SNPdbers796053075
MSV3drs796053075
GWAS Ctlgrs796053075
Max Magnitude0
ClinVar
Risk rs796053075(;)
Alt rs796053075(;)
Reference rs796053075(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166929992delT
CLNSRC
CLNACC RCV000189055.1,