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rs796052999

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052999(A;A)
Make rs796052999(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012104
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796052999
ebirs796052999
HLIrs796052999
Exacrs796052999
Varsomers796052999
Maprs796052999
PheGenIrs796052999
hapmaprs796052999
1000 genomesrs796052999
hgdprs796052999
ensemblrs796052999
gopubmedrs796052999
geneviewrs796052999
scholarrs796052999
googlers796052999
pharmgkbrs796052999
gwascentralrs796052999
openSNPrs796052999
23andMers796052999
23andMe allrs796052999
SNP Nexus

SNPshotrs796052999
SNPdbers796052999
MSV3drs796052999
GWAS Ctlgrs796052999
Max Magnitude0
ClinVar
Risk rs796052999(A;A)
Alt rs796052999(A;A)
Reference rs796052999(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868614C>T
CLNSRC
CLNACC RCV000188930.2,