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rs786205571

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205571(A;A)
Make rs786205571(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position113356462
GeneANK2
is asnp
is mentioned by
dbSNPrs786205571
ebirs786205571
HLIrs786205571
Exacrs786205571
Varsomers786205571
Maprs786205571
PheGenIrs786205571
hapmaprs786205571
1000 genomesrs786205571
hgdprs786205571
ensemblrs786205571
gopubmedrs786205571
geneviewrs786205571
scholarrs786205571
googlers786205571
pharmgkbrs786205571
gwascentralrs786205571
openSNPrs786205571
23andMers786205571
23andMe allrs786205571
SNP Nexus

SNPshotrs786205571
SNPdbers786205571
MSV3drs786205571
GWAS Ctlgrs786205571
Max Magnitude0
ClinVar
Risk rs786205571(A;A)
Alt rs786205571(A;A)
Reference rs786205571(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANK2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.114277618C>A
CLNSRC
CLNACC RCV000171380.1,