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rs886041991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position147562179
GeneCNTNAP2, LOC107986721
is asnp
is mentioned by
dbSNPrs886041991
dbSNP (classic)rs886041991
ClinGenrs886041991
ebirs886041991
HLIrs886041991
Exacrs886041991
Gnomadrs886041991
Varsomers886041991
LitVarrs886041991
Maprs886041991
PheGenIrs886041991
Biobankrs886041991
1000 genomesrs886041991
hgdprs886041991
ensemblrs886041991
geneviewrs886041991
scholarrs886041991
googlers886041991
pharmgkbrs886041991
gwascentralrs886041991
openSNPrs886041991
23andMers886041991
23andMe allrs886041991
SNPshotrs886041991
SNPdbers886041991
MSV3drs886041991
GWAS Ctlgrs886041991
Max Magnitude0
ClinVar
Risk rs886041991(T;T)
Alt rs886041991(T;T)
Reference Rs886041991(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.147259271C>T
CLNSRC
CLNACC RCV000264586.1,