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rs1057520743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520743(C;G)
Make rs1057520743(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position147128829
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1057520743
dbSNP (old)rs1057520743
ClinGenrs1057520743
ebirs1057520743
HLIrs1057520743
Exacrs1057520743
Gnomadrs1057520743
Varsomers1057520743
LitVarrs1057520743
Maprs1057520743
PheGenIrs1057520743
Biobankrs1057520743
1000 genomesrs1057520743
hgdprs1057520743
ensemblrs1057520743
gopubmedrs1057520743
geneviewrs1057520743
scholarrs1057520743
googlers1057520743
pharmgkbrs1057520743
gwascentralrs1057520743
openSNPrs1057520743
23andMers1057520743
23andMe allrs1057520743
SNPshotrs1057520743
SNPdbers1057520743
MSV3drs1057520743
GWAS Ctlgrs1057520743
Max Magnitude0
ClinVar
Risk rs1057520743(G;G)
Alt rs1057520743(G;G)
Reference Rs1057520743(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.146825921C>G
CLNSRC
CLNACC RCV000421673.1,