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rs786205724

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205724(C;T)
Make rs786205724(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position113282730
GeneANK2
is asnp
is mentioned by
dbSNPrs786205724
ebirs786205724
HLIrs786205724
Exacrs786205724
Varsomers786205724
Maprs786205724
PheGenIrs786205724
hapmaprs786205724
1000 genomesrs786205724
hgdprs786205724
ensemblrs786205724
gopubmedrs786205724
geneviewrs786205724
scholarrs786205724
googlers786205724
pharmgkbrs786205724
gwascentralrs786205724
openSNPrs786205724
23andMers786205724
23andMe allrs786205724
SNP Nexus

SNPshotrs786205724
SNPdbers786205724
MSV3drs786205724
GWAS Ctlgrs786205724
Max Magnitude0
ClinVar
Risk rs786205724(T;T)
Alt rs786205724(T;T)
Reference rs786205724(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANK2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.114203886C>T
CLNSRC
CLNACC RCV000170682.4,