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rs796053049

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053049(A;G)
Make rs796053049(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991469
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053049
ebirs796053049
HLIrs796053049
Exacrs796053049
Varsomers796053049
Maprs796053049
PheGenIrs796053049
hapmaprs796053049
1000 genomesrs796053049
hgdprs796053049
ensemblrs796053049
gopubmedrs796053049
geneviewrs796053049
scholarrs796053049
googlers796053049
pharmgkbrs796053049
gwascentralrs796053049
openSNPrs796053049
23andMers796053049
23andMe allrs796053049
SNP Nexus

SNPshotrs796053049
SNPdbers796053049
MSV3drs796053049
GWAS Ctlgrs796053049
Max Magnitude0
ClinVar
Risk rs796053049(G;G)
Alt rs796053049(G;G)
Reference rs796053049(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166847979T>C
CLNSRC
CLNACC RCV000189022.1,