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rs587778980

From SNPedia

Orientationplus
Geno Mag Summary
(GTGCCTG;GTGCCTG) 0 common in clinvar
Make rs587778980(-;-)
Make rs587778980(-;TGCCTGG)
Make rs587778980(TGCCTGG;TGCCTGG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050493
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778980
ebirs587778980
HLIrs587778980
Exacrs587778980
Varsomers587778980
Maprs587778980
PheGenIrs587778980
hapmaprs587778980
1000 genomesrs587778980
hgdprs587778980
ensemblrs587778980
gopubmedrs587778980
geneviewrs587778980
scholarrs587778980
googlers587778980
pharmgkbrs587778980
gwascentralrs587778980
openSNPrs587778980
23andMers587778980
23andMe allrs587778980
SNP Nexus

SNPshotrs587778980
SNPdbers587778980
MSV3drs587778980
GWAS Ctlgrs587778980
Max Magnitude0
ClinVar
Risk rs587778980(;)
Alt rs587778980(;)
Reference rs587778980(GTGCCTG;GTGCCTG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37091984_37091990delTGCCTGG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075547.2,