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rs786205085

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205085(A;A)
Make rs786205085(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position39026811
GeneADAM9
is asnp
is mentioned by
dbSNPrs786205085
ebirs786205085
HLIrs786205085
Exacrs786205085
Varsomers786205085
Maprs786205085
PheGenIrs786205085
hapmaprs786205085
1000 genomesrs786205085
hgdprs786205085
ensemblrs786205085
gopubmedrs786205085
geneviewrs786205085
scholarrs786205085
googlers786205085
pharmgkbrs786205085
gwascentralrs786205085
openSNPrs786205085
23andMers786205085
23andMe allrs786205085
SNP Nexus

SNPshotrs786205085
SNPdbers786205085
MSV3drs786205085
GWAS Ctlgrs786205085
Max Magnitude0
ClinVar
Risk rs786205085(A;A)
Alt rs786205085(A;A)
Reference rs786205085(G;G)
Significance Pathogenic
Disease Cone-rod dystrophy 9
Variation info
Gene ADAM9
CLNDBN Cone-rod dystrophy 9
Reversed 0
HGVS NC_000008.10:g.38884330G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007279.3,