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rs786205535

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205535(C;G)
Make rs786205535(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position112021494
GeneMERTK
is asnp
is mentioned by
dbSNPrs786205535
ebirs786205535
HLIrs786205535
Exacrs786205535
Varsomers786205535
Maprs786205535
PheGenIrs786205535
hapmaprs786205535
1000 genomesrs786205535
hgdprs786205535
ensemblrs786205535
gopubmedrs786205535
geneviewrs786205535
scholarrs786205535
googlers786205535
pharmgkbrs786205535
gwascentralrs786205535
openSNPrs786205535
23andMers786205535
23andMe allrs786205535
SNP Nexus

SNPshotrs786205535
SNPdbers786205535
MSV3drs786205535
GWAS Ctlgrs786205535
Max Magnitude0
ClinVar
Risk rs786205535(G;G)
Alt rs786205535(G;G)
Reference rs786205535(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MERTK
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.112779071C>G
CLNSRC
CLNACC RCV000171305.1,