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rs1057520844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520844(A;A)
Make rs1057520844(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165388710
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057520844
dbSNP (old)rs1057520844
ClinGenrs1057520844
ebirs1057520844
HLIrs1057520844
Exacrs1057520844
Gnomadrs1057520844
Varsomers1057520844
LitVarrs1057520844
Maprs1057520844
PheGenIrs1057520844
Biobankrs1057520844
1000 genomesrs1057520844
hgdprs1057520844
ensemblrs1057520844
gopubmedrs1057520844
geneviewrs1057520844
scholarrs1057520844
googlers1057520844
pharmgkbrs1057520844
gwascentralrs1057520844
openSNPrs1057520844
23andMers1057520844
23andMe allrs1057520844
SNPshotrs1057520844
SNPdbers1057520844
MSV3drs1057520844
GWAS Ctlgrs1057520844
Max Magnitude0
ClinVar
Risk rs1057520844(A;A)
Alt rs1057520844(A;A)
Reference Rs1057520844(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245220G>A
CLNSRC
CLNACC RCV000433186.1,