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rs587780683

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780683(-;-)
Make rs587780683(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050572
GeneMLH1
is asnp
is mentioned by
dbSNPrs587780683
ebirs587780683
HLIrs587780683
Exacrs587780683
Varsomers587780683
Maprs587780683
PheGenIrs587780683
hapmaprs587780683
1000 genomesrs587780683
hgdprs587780683
ensemblrs587780683
gopubmedrs587780683
geneviewrs587780683
scholarrs587780683
googlers587780683
pharmgkbrs587780683
gwascentralrs587780683
openSNPrs587780683
23andMers587780683
23andMe allrs587780683
SNP Nexus

SNPshotrs587780683
SNPdbers587780683
MSV3drs587780683
GWAS Ctlgrs587780683
Max Magnitude0
ClinVar
Risk rs587780683(;)
Alt rs587780683(;)
Reference rs587780683(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092063delT
CLNSRC
CLNACC RCV000122975.1,