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rs398124268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124268(A;A)
Make rs398124268(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position147903619
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs398124268
ebirs398124268
HLIrs398124268
Exacrs398124268
Varsomers398124268
Maprs398124268
PheGenIrs398124268
hapmaprs398124268
1000 genomesrs398124268
hgdprs398124268
ensemblrs398124268
gopubmedrs398124268
geneviewrs398124268
scholarrs398124268
googlers398124268
pharmgkbrs398124268
gwascentralrs398124268
openSNPrs398124268
23andMers398124268
23andMe allrs398124268
SNP Nexus

SNPshotrs398124268
SNPdbers398124268
MSV3drs398124268
GWAS Ctlgrs398124268
Max Magnitude0
ClinVar
Risk rs398124268(A;A)
Alt rs398124268(A;A)
Reference rs398124268(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.147600711G>A
CLNSRC HGMD
CLNACC RCV000081591.5,