Have questions? Visit https://www.reddit.com/r/SNPedia

rs767146880

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767146880(A;A)
Make rs767146880(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position70810048
GeneMIR204, TRPM3
is asnp
is mentioned by
dbSNPrs767146880
ebirs767146880
HLIrs767146880
Exacrs767146880
Varsomers767146880
Maprs767146880
PheGenIrs767146880
hapmaprs767146880
1000 genomesrs767146880
hgdprs767146880
ensemblrs767146880
gopubmedrs767146880
geneviewrs767146880
scholarrs767146880
googlers767146880
pharmgkbrs767146880
gwascentralrs767146880
openSNPrs767146880
23andMers767146880
23andMe allrs767146880
SNP Nexus

SNPshotrs767146880
SNPdbers767146880
MSV3drs767146880
GWAS Ctlgrs767146880
Max Magnitude0
ClinVar
Risk rs767146880(A,C;A,C)
Alt rs767146880(A,C;A,C)
Reference rs767146880(G;G)
Significance Pathogenic
Disease Retinal dystrophy and iris coloboma with or without congenital cataract
Variation info
Gene TRPM3 MIR204
CLNDBN Retinal dystrophy and iris coloboma with or without congenital cataract
Reversed 0
HGVS NC_000009.11:g.73424964G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203227.1,