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rs1057518048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518048(A;A)
Make rs1057518048(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165344757
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057518048
dbSNP (old)rs1057518048
ClinGenrs1057518048
ebirs1057518048
HLIrs1057518048
Exacrs1057518048
Gnomadrs1057518048
Varsomers1057518048
LitVarrs1057518048
Maprs1057518048
PheGenIrs1057518048
Biobankrs1057518048
1000 genomesrs1057518048
hgdprs1057518048
ensemblrs1057518048
gopubmedrs1057518048
geneviewrs1057518048
scholarrs1057518048
googlers1057518048
pharmgkbrs1057518048
gwascentralrs1057518048
openSNPrs1057518048
23andMers1057518048
23andMe allrs1057518048
SNPshotrs1057518048
SNPdbers1057518048
MSV3drs1057518048
GWAS Ctlgrs1057518048
Max Magnitude0
ClinVar
Risk rs1057518048(A;A)
Alt rs1057518048(A;A)
Reference Rs1057518048(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201267G>A
CLNSRC
CLNACC RCV000414442.1,