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rs879255520

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255520(-;-)
Make rs879255520(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position186001391
GeneHMCN1
is asnp
is mentioned by
dbSNPrs879255520
ebirs879255520
HLIrs879255520
Exacrs879255520
Varsomers879255520
Maprs879255520
PheGenIrs879255520
hapmaprs879255520
1000 genomesrs879255520
hgdprs879255520
ensemblrs879255520
gopubmedrs879255520
geneviewrs879255520
scholarrs879255520
googlers879255520
pharmgkbrs879255520
gwascentralrs879255520
openSNPrs879255520
23andMers879255520
23andMe allrs879255520
SNP Nexus

SNPshotrs879255520
SNPdbers879255520
MSV3drs879255520
GWAS Ctlgrs879255520
Max Magnitude0
ClinVar
Risk rs879255520(;)
Alt rs879255520(;)
Reference rs879255520(C;C)
Significance Pathogenic
Disease Age-related macular degeneration 1
Variation info
Gene HMCN1
CLNDBN Age-related macular degeneration 1
Reversed 0
HGVS NC_000001.10:g.185970523delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000201932.2,