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rs786205487

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205487(A;T)
Make rs786205487(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position50620724
GeneATL1
is asnp
is mentioned by
dbSNPrs786205487
ebirs786205487
HLIrs786205487
Exacrs786205487
Varsomers786205487
Maprs786205487
PheGenIrs786205487
hapmaprs786205487
1000 genomesrs786205487
hgdprs786205487
ensemblrs786205487
gopubmedrs786205487
geneviewrs786205487
scholarrs786205487
googlers786205487
pharmgkbrs786205487
gwascentralrs786205487
openSNPrs786205487
23andMers786205487
23andMe allrs786205487
SNP Nexus

SNPshotrs786205487
SNPdbers786205487
MSV3drs786205487
GWAS Ctlgrs786205487
Max Magnitude0
ClinVar
Risk rs786205487(T;T)
Alt rs786205487(T;T)
Reference rs786205487(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATL1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.51087442A>T
CLNSRC
CLNACC RCV000171222.1,