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rs786205086

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205086(A;G)
Make rs786205086(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position39017211
GeneADAM9
is asnp
is mentioned by
dbSNPrs786205086
ebirs786205086
HLIrs786205086
Exacrs786205086
Varsomers786205086
Maprs786205086
PheGenIrs786205086
hapmaprs786205086
1000 genomesrs786205086
hgdprs786205086
ensemblrs786205086
gopubmedrs786205086
geneviewrs786205086
scholarrs786205086
googlers786205086
pharmgkbrs786205086
gwascentralrs786205086
openSNPrs786205086
23andMers786205086
23andMe allrs786205086
SNP Nexus

SNPshotrs786205086
SNPdbers786205086
MSV3drs786205086
GWAS Ctlgrs786205086
Max Magnitude0
ClinVar
Risk rs786205086(G;G)
Alt rs786205086(G;G)
Reference rs786205086(A;A)
Significance Pathogenic
Disease Cone-rod dystrophy 9
Variation info
Gene ADAM9
CLNDBN Cone-rod dystrophy 9
Reversed 0
HGVS NC_000008.10:g.38874730A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007282.3,