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rs587776769

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776769(-;-)
Make rs587776769(-;TG)
Make rs587776769(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position30691497
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs587776769
ebirs587776769
HLIrs587776769
Exacrs587776769
Varsomers587776769
Maprs587776769
PheGenIrs587776769
hapmaprs587776769
1000 genomesrs587776769
hgdprs587776769
ensemblrs587776769
gopubmedrs587776769
geneviewrs587776769
scholarrs587776769
googlers587776769
pharmgkbrs587776769
gwascentralrs587776769
openSNPrs587776769
23andMers587776769
23andMe allrs587776769
SNP Nexus

SNPshotrs587776769
SNPdbers587776769
MSV3drs587776769
GWAS Ctlgrs587776769
Max Magnitude0
ClinVar
Risk rs587776769(GT;GT)
Alt rs587776769(GT;GT)
Reference rs587776769(;)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 6
Variation info
Gene TGFBR2
CLNDBN Hereditary nonpolyposis colorectal cancer type 6
Reversed 0
HGVS NC_000003.11:g.30732988_30732989dupTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013324.4,