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rs752550849

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752550849(C;T)
Make rs752550849(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position147300239
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs752550849
ebirs752550849
HLIrs752550849
Exacrs752550849
Varsomers752550849
Maprs752550849
PheGenIrs752550849
hapmaprs752550849
1000 genomesrs752550849
hgdprs752550849
ensemblrs752550849
gopubmedrs752550849
geneviewrs752550849
scholarrs752550849
googlers752550849
pharmgkbrs752550849
gwascentralrs752550849
openSNPrs752550849
23andMers752550849
23andMe allrs752550849
SNP Nexus

SNPshotrs752550849
SNPdbers752550849
MSV3drs752550849
GWAS Ctlgrs752550849
Max Magnitude0
ClinVar
Risk rs752550849(G,T;G,T)
Alt rs752550849(G,T;G,T)
Reference rs752550849(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.146997331C>T
CLNSRC
CLNACC RCV000187185.1,