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rs796053206

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs796053206(GC;TT)
Make rs796053206(TT;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165310343
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053206
ebirs796053206
HLIrs796053206
Exacrs796053206
Varsomers796053206
Maprs796053206
PheGenIrs796053206
hapmaprs796053206
1000 genomesrs796053206
hgdprs796053206
ensemblrs796053206
gopubmedrs796053206
geneviewrs796053206
scholarrs796053206
googlers796053206
pharmgkbrs796053206
gwascentralrs796053206
openSNPrs796053206
23andMers796053206
23andMe allrs796053206
SNP Nexus

SNPshotrs796053206
SNPdbers796053206
MSV3drs796053206
GWAS Ctlgrs796053206
Max Magnitude0
ClinVar
Risk rs796053206(TT;TT)
Alt rs796053206(TT;TT)
Reference rs796053206(GC;GC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166853_166166854delGCinsTT
CLNSRC
CLNACC RCV000189248.1,