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rs786205534

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205534(G;G)
Make rs786205534(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position111997478
GeneMERTK
is asnp
is mentioned by
dbSNPrs786205534
ebirs786205534
HLIrs786205534
Exacrs786205534
Varsomers786205534
Maprs786205534
PheGenIrs786205534
hapmaprs786205534
1000 genomesrs786205534
hgdprs786205534
ensemblrs786205534
gopubmedrs786205534
geneviewrs786205534
scholarrs786205534
googlers786205534
pharmgkbrs786205534
gwascentralrs786205534
openSNPrs786205534
23andMers786205534
23andMe allrs786205534
SNP Nexus

SNPshotrs786205534
SNPdbers786205534
MSV3drs786205534
GWAS Ctlgrs786205534
Max Magnitude0
ClinVar
Risk rs786205534(G;G)
Alt rs786205534(G;G)
Reference rs786205534(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MERTK
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.112755055T>G
CLNSRC
CLNACC RCV000171304.1,