Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521747(C;C)
Make rs1057521747(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165386976
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057521747
dbSNP (classic)rs1057521747
ClinGenrs1057521747
ebirs1057521747
HLIrs1057521747
Exacrs1057521747
Gnomadrs1057521747
Varsomers1057521747
LitVarrs1057521747
Maprs1057521747
PheGenIrs1057521747
Biobankrs1057521747
1000 genomesrs1057521747
hgdprs1057521747
ensemblrs1057521747
geneviewrs1057521747
scholarrs1057521747
googlers1057521747
pharmgkbrs1057521747
gwascentralrs1057521747
openSNPrs1057521747
23andMers1057521747
23andMe allrs1057521747
SNPshotrs1057521747
SNPdbers1057521747
MSV3drs1057521747
GWAS Ctlgrs1057521747
Max Magnitude0
ClinVar
Risk rs1057521747(C;C)
Alt rs1057521747(C;C)
Reference Rs1057521747(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243486G>C
CLNSRC
CLNACC RCV000432281.1,