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rs786205461

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205461(C;T)
Make rs786205461(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position90915602
GeneANKRD1
is asnp
is mentioned by
dbSNPrs786205461
ebirs786205461
HLIrs786205461
Exacrs786205461
Varsomers786205461
Maprs786205461
PheGenIrs786205461
hapmaprs786205461
1000 genomesrs786205461
hgdprs786205461
ensemblrs786205461
gopubmedrs786205461
geneviewrs786205461
scholarrs786205461
googlers786205461
pharmgkbrs786205461
gwascentralrs786205461
openSNPrs786205461
23andMers786205461
23andMe allrs786205461
SNP Nexus

SNPshotrs786205461
SNPdbers786205461
MSV3drs786205461
GWAS Ctlgrs786205461
Max Magnitude0
ClinVar
Risk rs786205461(T;T)
Alt rs786205461(T;T)
Reference rs786205461(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANKRD1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.92675359G>A
CLNSRC
CLNACC RCV000171183.1,