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rs372425457

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372425457(A;A)
Make rs372425457(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165996038
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs372425457
ebirs372425457
HLIrs372425457
Exacrs372425457
Varsomers372425457
Maprs372425457
PheGenIrs372425457
hapmaprs372425457
1000 genomesrs372425457
hgdprs372425457
ensemblrs372425457
gopubmedrs372425457
geneviewrs372425457
scholarrs372425457
googlers372425457
pharmgkbrs372425457
gwascentralrs372425457
openSNPrs372425457
23andMers372425457
23andMe allrs372425457
SNP Nexus

SNPshotrs372425457
SNPdbers372425457
MSV3drs372425457
GWAS Ctlgrs372425457
Max Magnitude0
ClinVar
Risk rs372425457(A;A)
Alt rs372425457(A;A)
Reference rs372425457(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166852548G>A
CLNSRC
CLNACC RCV000188964.2,