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rs796053194

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs796053194(-;-)
Make rs796053194(-;GAA)
Make rs796053194(GAA;GAA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165381123
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053194
ebirs796053194
HLIrs796053194
Exacrs796053194
Varsomers796053194
Maprs796053194
PheGenIrs796053194
hapmaprs796053194
1000 genomesrs796053194
hgdprs796053194
ensemblrs796053194
gopubmedrs796053194
geneviewrs796053194
scholarrs796053194
googlers796053194
pharmgkbrs796053194
gwascentralrs796053194
openSNPrs796053194
23andMers796053194
23andMe allrs796053194
SNP Nexus

SNPshotrs796053194
SNPdbers796053194
MSV3drs796053194
GWAS Ctlgrs796053194
Max Magnitude0
ClinVar
Risk rs796053194(;)
Alt rs796053194(;)
Reference rs796053194(AGA;AGA)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237633_166237635delGAA
CLNSRC
CLNACC RCV000189232.1,