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rs137853148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853148(C;T)
Make rs137853148(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position17589479
GenePDGFRL
is asnp
is mentioned by
dbSNPrs137853148
ebirs137853148
HLIrs137853148
Exacrs137853148
Varsomers137853148
Maprs137853148
PheGenIrs137853148
hapmaprs137853148
1000 genomesrs137853148
hgdprs137853148
ensemblrs137853148
gopubmedrs137853148
geneviewrs137853148
scholarrs137853148
googlers137853148
pharmgkbrs137853148
gwascentralrs137853148
openSNPrs137853148
23andMers137853148
23andMe allrs137853148
SNP Nexus

SNPshotrs137853148
SNPdbers137853148
MSV3drs137853148
GWAS Ctlgrs137853148
Max Magnitude0
OMIM604584
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853148(T;T)
Alt rs137853148(T;T)
Reference rs137853148(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PDGFRL
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000008.10:g.17446988C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005802.4,