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rs796053082

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053082(-;-)
Make rs796053082(-;A)
Make rs796053082(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996039
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053082
ebirs796053082
HLIrs796053082
Exacrs796053082
Varsomers796053082
Maprs796053082
PheGenIrs796053082
hapmaprs796053082
1000 genomesrs796053082
hgdprs796053082
ensemblrs796053082
gopubmedrs796053082
geneviewrs796053082
scholarrs796053082
googlers796053082
pharmgkbrs796053082
gwascentralrs796053082
openSNPrs796053082
23andMers796053082
23andMe allrs796053082
SNP Nexus

SNPshotrs796053082
SNPdbers796053082
MSV3drs796053082
GWAS Ctlgrs796053082
Max Magnitude0
ClinVar
Risk rs796053082(A;A)
Alt rs796053082(A;A)
Reference rs796053082(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852550dupT
CLNSRC
CLNACC RCV000189062.1,