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rs137853041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853041(C;T)
Make rs137853041(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position39017298
GeneADAM9
is asnp
is mentioned by
dbSNPrs137853041
ebirs137853041
HLIrs137853041
Exacrs137853041
Varsomers137853041
Maprs137853041
PheGenIrs137853041
hapmaprs137853041
1000 genomesrs137853041
hgdprs137853041
ensemblrs137853041
gopubmedrs137853041
geneviewrs137853041
scholarrs137853041
googlers137853041
pharmgkbrs137853041
gwascentralrs137853041
openSNPrs137853041
23andMers137853041
23andMe allrs137853041
SNP Nexus

SNPshotrs137853041
SNPdbers137853041
MSV3drs137853041
GWAS Ctlgrs137853041
Max Magnitude0
OMIM602713
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853041(G,T;G,T)
Alt rs137853041(G,T;G,T)
Reference rs137853041(C;C)
Significance Pathogenic
Disease Cone-rod dystrophy 9
Variation info
Gene ADAM9
CLNDBN Cone-rod dystrophy 9
Reversed 0
HGVS NC_000008.10:g.38874817C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007281.3,