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rs137853277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853277(C;T)
Make rs137853277(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position171636382
GeneMYOC
is asnp
is mentioned by
dbSNPrs137853277
ebirs137853277
HLIrs137853277
Exacrs137853277
Varsomers137853277
Maprs137853277
PheGenIrs137853277
hapmaprs137853277
1000 genomesrs137853277
hgdprs137853277
ensemblrs137853277
gopubmedrs137853277
geneviewrs137853277
scholarrs137853277
googlers137853277
pharmgkbrs137853277
gwascentralrs137853277
openSNPrs137853277
23andMers137853277
23andMe allrs137853277
SNP Nexus

SNPshotrs137853277
SNPdbers137853277
MSV3drs137853277
GWAS Ctlgrs137853277
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs137853277(T;T)
Alt rs137853277(T;T)
Reference rs137853277(C;C)
Significance Untested
Disease
Variation info
Gene MYOC
CLNDBN OMIM
Reversed 1
HGVS NC_000001.10:g.171605522G>A
CLNSRC
CLNACC


OMIM601652
Desc
Variant
Relatedalso