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rs534934297

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs534934297(A;G)
Make rs534934297(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position113356942
GeneANK2
is asnp
is mentioned by
dbSNPrs534934297
ebirs534934297
HLIrs534934297
Exacrs534934297
Varsomers534934297
Maprs534934297
PheGenIrs534934297
hapmaprs534934297
1000 genomesrs534934297
hgdprs534934297
ensemblrs534934297
gopubmedrs534934297
geneviewrs534934297
scholarrs534934297
googlers534934297
pharmgkbrs534934297
gwascentralrs534934297
openSNPrs534934297
23andMers534934297
23andMe allrs534934297
SNP Nexus

SNPshotrs534934297
SNPdbers534934297
MSV3drs534934297
GWAS Ctlgrs534934297
Max Magnitude0
ClinVar
Risk rs534934297(G;G)
Alt rs534934297(G;G)
Reference rs534934297(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANK2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.114278098A>G
CLNSRC
CLNACC RCV000171381.1,