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rs201076428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs201076428(C;T)
Make rs201076428(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome7
Position147639254
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs201076428
dbSNP (classic)rs201076428
ClinGenrs201076428
ebirs201076428
HLIrs201076428
Exacrs201076428
Gnomadrs201076428
Varsomers201076428
LitVarrs201076428
Maprs201076428
PheGenIrs201076428
Biobankrs201076428
1000 genomesrs201076428
hgdprs201076428
ensemblrs201076428
geneviewrs201076428
scholarrs201076428
googlers201076428
pharmgkbrs201076428
gwascentralrs201076428
openSNPrs201076428
23andMers201076428
23andMe allrs201076428
SNPshotrs201076428
SNPdbers201076428
MSV3drs201076428
GWAS Ctlgrs201076428
Max Magnitude0

OMIM pathogenic variant