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rs121434382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121434382(A;G)
Make rs121434382(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position186178506
GeneHMCN1
is asnp
is mentioned by
dbSNPrs121434382
ebirs121434382
HLIrs121434382
Exacrs121434382
Varsomers121434382
Maprs121434382
PheGenIrs121434382
hapmaprs121434382
1000 genomesrs121434382
hgdprs121434382
ensemblrs121434382
gopubmedrs121434382
geneviewrs121434382
scholarrs121434382
googlers121434382
pharmgkbrs121434382
gwascentralrs121434382
openSNPrs121434382
23andMers121434382
23andMe allrs121434382
SNP Nexus

SNPshotrs121434382
SNPdbers121434382
MSV3drs121434382
GWAS Ctlgrs121434382
Max Magnitude0
OMIM608548
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434382(G;G)
Alt rs121434382(G;G)
Reference rs121434382(A;A)
Significance Other
Disease MACULAR DEGENERATION
Variation info
Gene HMCN1
CLNDBN MACULAR DEGENERATION, AGE-RELATED, 1, SUSCEPTIBILITY TO
Reversed 0
HGVS NC_000001.10:g.186147638A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002289.2,