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rs730880273

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880273(A;G)
Make rs730880273(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position112001199
GeneMERTK
is asnp
is mentioned by
dbSNPrs730880273
ebirs730880273
HLIrs730880273
Exacrs730880273
Varsomers730880273
Maprs730880273
PheGenIrs730880273
hapmaprs730880273
1000 genomesrs730880273
hgdprs730880273
ensemblrs730880273
gopubmedrs730880273
geneviewrs730880273
scholarrs730880273
googlers730880273
pharmgkbrs730880273
gwascentralrs730880273
openSNPrs730880273
23andMers730880273
23andMe allrs730880273
SNP Nexus

SNPshotrs730880273
SNPdbers730880273
MSV3drs730880273
GWAS Ctlgrs730880273
Max Magnitude0
ClinVar
Risk rs730880273(G;G)
Alt rs730880273(G;G)
Reference rs730880273(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 38
Variation info
Gene MERTK
CLNDBN Retinitis pigmentosa 38
Reversed 0
HGVS NC_000002.11:g.112758776A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005732.3,