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rs761413864

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs761413864(A;G)
Make rs761413864(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position113282867
GeneANK2
is asnp
is mentioned by
dbSNPrs761413864
ebirs761413864
HLIrs761413864
Exacrs761413864
Varsomers761413864
Maprs761413864
PheGenIrs761413864
hapmaprs761413864
1000 genomesrs761413864
hgdprs761413864
ensemblrs761413864
gopubmedrs761413864
geneviewrs761413864
scholarrs761413864
googlers761413864
pharmgkbrs761413864
gwascentralrs761413864
openSNPrs761413864
23andMers761413864
23andMe allrs761413864
SNP Nexus

SNPshotrs761413864
SNPdbers761413864
MSV3drs761413864
GWAS Ctlgrs761413864
Max Magnitude0
ClinVar
Risk rs761413864(G;G)
Alt rs761413864(G;G)
Reference rs761413864(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANK2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.114204023A>G
CLNSRC
CLNACC RCV000170729.3,