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rs796053154

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053154(A;A)
Make rs796053154(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165387016
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053154
ebirs796053154
HLIrs796053154
Exacrs796053154
Varsomers796053154
Maprs796053154
PheGenIrs796053154
hapmaprs796053154
1000 genomesrs796053154
hgdprs796053154
ensemblrs796053154
gopubmedrs796053154
geneviewrs796053154
scholarrs796053154
googlers796053154
pharmgkbrs796053154
gwascentralrs796053154
openSNPrs796053154
23andMers796053154
23andMe allrs796053154
SNP Nexus

SNPshotrs796053154
SNPdbers796053154
MSV3drs796053154
GWAS Ctlgrs796053154
Max Magnitude0
ClinVar
Risk rs796053154(A;A)
Alt rs796053154(A;A)
Reference rs796053154(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243526G>A
CLNSRC
CLNACC RCV000189168.2,