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rs786205151

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205151(A;G)
Make rs786205151(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position39055575
GeneADAM9
is asnp
is mentioned by
dbSNPrs786205151
ebirs786205151
HLIrs786205151
Exacrs786205151
Varsomers786205151
Maprs786205151
PheGenIrs786205151
hapmaprs786205151
1000 genomesrs786205151
hgdprs786205151
ensemblrs786205151
gopubmedrs786205151
geneviewrs786205151
scholarrs786205151
googlers786205151
pharmgkbrs786205151
gwascentralrs786205151
openSNPrs786205151
23andMers786205151
23andMe allrs786205151
SNP Nexus

SNPshotrs786205151
SNPdbers786205151
MSV3drs786205151
GWAS Ctlgrs786205151
Max Magnitude0
ClinVar
Risk rs786205151(G;G)
Alt rs786205151(G;G)
Reference rs786205151(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.38913094A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170309.3,