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rs796053056

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053056(-;-)
Make rs796053056(-;GTAGA)
Make rs796053056(GTAGA;GTAGA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166046899
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053056
ebirs796053056
HLIrs796053056
Exacrs796053056
Varsomers796053056
Maprs796053056
PheGenIrs796053056
hapmaprs796053056
1000 genomesrs796053056
hgdprs796053056
ensemblrs796053056
gopubmedrs796053056
geneviewrs796053056
scholarrs796053056
googlers796053056
pharmgkbrs796053056
gwascentralrs796053056
openSNPrs796053056
23andMers796053056
23andMe allrs796053056
SNP Nexus

SNPshotrs796053056
SNPdbers796053056
MSV3drs796053056
GWAS Ctlgrs796053056
Max Magnitude0
ClinVar
Risk rs796053056(GTAGA;GTAGA)
Alt rs796053056(GTAGA;GTAGA)
Reference rs796053056(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903409_166903410insTCTAC
CLNSRC
CLNACC RCV000189036.1,