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rs786205533

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205533(A;T)
Make rs786205533(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position111929383
GeneMERTK
is asnp
is mentioned by
dbSNPrs786205533
ebirs786205533
HLIrs786205533
Exacrs786205533
Varsomers786205533
Maprs786205533
PheGenIrs786205533
hapmaprs786205533
1000 genomesrs786205533
hgdprs786205533
ensemblrs786205533
gopubmedrs786205533
geneviewrs786205533
scholarrs786205533
googlers786205533
pharmgkbrs786205533
gwascentralrs786205533
openSNPrs786205533
23andMers786205533
23andMe allrs786205533
SNP Nexus

SNPshotrs786205533
SNPdbers786205533
MSV3drs786205533
GWAS Ctlgrs786205533
Max Magnitude0
ClinVar
Risk rs786205533(T;T)
Alt rs786205533(T;T)
Reference rs786205533(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MERTK
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.112686960A>T
CLNSRC
CLNACC RCV000171303.1,