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rs750151209

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs750151209(-;-)
Make rs750151209(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position181548785
GeneCERKL
is asnp
is mentioned by
dbSNPrs750151209
ebirs750151209
HLIrs750151209
Exacrs750151209
Varsomers750151209
Maprs750151209
PheGenIrs750151209
hapmaprs750151209
1000 genomesrs750151209
hgdprs750151209
ensemblrs750151209
gopubmedrs750151209
geneviewrs750151209
scholarrs750151209
googlers750151209
pharmgkbrs750151209
gwascentralrs750151209
openSNPrs750151209
23andMers750151209
23andMe allrs750151209
SNP Nexus

SNPshotrs750151209
SNPdbers750151209
MSV3drs750151209
GWAS Ctlgrs750151209
Max Magnitude0
ClinVar
Risk rs750151209(;)
Alt rs750151209(;)
Reference rs750151209(AT;AT)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CERKL
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000002.11:g.182413512_182413513delAT
CLNSRC
CLNACC RCV000225454.1,