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rs137853040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853040(C;T)
Make rs137853040(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position39023177
GeneADAM9
is asnp
is mentioned by
dbSNPrs137853040
ebirs137853040
HLIrs137853040
Exacrs137853040
Varsomers137853040
Maprs137853040
PheGenIrs137853040
hapmaprs137853040
1000 genomesrs137853040
hgdprs137853040
ensemblrs137853040
gopubmedrs137853040
geneviewrs137853040
scholarrs137853040
googlers137853040
pharmgkbrs137853040
gwascentralrs137853040
openSNPrs137853040
23andMers137853040
23andMe allrs137853040
SNP Nexus

SNPshotrs137853040
SNPdbers137853040
MSV3drs137853040
GWAS Ctlgrs137853040
Max Magnitude0
OMIM602713
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853040(T;T)
Alt rs137853040(T;T)
Reference rs137853040(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.38880696C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007280.3,