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rs371956016

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371956016(G;T)
Make rs371956016(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position112019523
GeneMERTK
is asnp
is mentioned by
dbSNPrs371956016
ClinGenrs371956016
ebirs371956016
HLIrs371956016
Exacrs371956016
Varsomers371956016
Maprs371956016
PheGenIrs371956016
hapmaprs371956016
1000 genomesrs371956016
hgdprs371956016
ensemblrs371956016
gopubmedrs371956016
geneviewrs371956016
scholarrs371956016
googlers371956016
pharmgkbrs371956016
gwascentralrs371956016
openSNPrs371956016
23andMers371956016
23andMe allrs371956016
SNP Nexus

SNPshotrs371956016
SNPdbers371956016
MSV3drs371956016
GWAS Ctlgrs371956016
Max Magnitude0
ClinVar
Risk rs371956016(T;T)
Alt rs371956016(T;T)
Reference Rs371956016(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 38
Variation info
Gene MERTK
CLNDBN Retinitis pigmentosa 38
Reversed 0
HGVS NC_000002.11:g.112777100G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005734.5,