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rs1057524573

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524573(C;C)
Make rs1057524573(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165344759
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057524573
dbSNP (old)rs1057524573
ClinGenrs1057524573
ebirs1057524573
HLIrs1057524573
Exacrs1057524573
Gnomadrs1057524573
Varsomers1057524573
Maprs1057524573
PheGenIrs1057524573
Biobankrs1057524573
1000 genomesrs1057524573
hgdprs1057524573
ensemblrs1057524573
gopubmedrs1057524573
geneviewrs1057524573
scholarrs1057524573
googlers1057524573
pharmgkbrs1057524573
gwascentralrs1057524573
openSNPrs1057524573
23andMers1057524573
23andMe allrs1057524573
SNPshotrs1057524573
SNPdbers1057524573
MSV3drs1057524573
GWAS Ctlgrs1057524573
Max Magnitude0
ClinVar
Risk rs1057524573(C;C)
Alt rs1057524573(C;C)
Reference Rs1057524573(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201269T>C
CLNSRC
CLNACC RCV000431611.1,