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rs137853112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853112(A;A)
Make rs137853112(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position23140775
GeneKLHL7
is asnp
is mentioned by
dbSNPrs137853112
ebirs137853112
HLIrs137853112
Exacrs137853112
Varsomers137853112
Maprs137853112
PheGenIrs137853112
hapmaprs137853112
1000 genomesrs137853112
hgdprs137853112
ensemblrs137853112
gopubmedrs137853112
geneviewrs137853112
scholarrs137853112
googlers137853112
pharmgkbrs137853112
gwascentralrs137853112
openSNPrs137853112
23andMers137853112
23andMe allrs137853112
SNP Nexus

SNPshotrs137853112
SNPdbers137853112
MSV3drs137853112
GWAS Ctlgrs137853112
Max Magnitude0
OMIM611119
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853112(A;A)
Alt rs137853112(A;A)
Reference rs137853112(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 42
Variation info
Gene KLHL7
CLNDBN Retinitis pigmentosa 42
Reversed 0
HGVS NC_000007.13:g.23180394G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001063.3,