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rs587779043

From SNPedia

Orientationplus
Geno Mag Summary
(TTCCT;TTCCT) 0 common in clinvar
Make rs587779043(-;-)
Make rs587779043(-;TCCTT)
Make rs587779043(TCCTT;TCCTT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017526
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779043
ebirs587779043
HLIrs587779043
Exacrs587779043
Varsomers587779043
Maprs587779043
PheGenIrs587779043
hapmaprs587779043
1000 genomesrs587779043
hgdprs587779043
ensemblrs587779043
gopubmedrs587779043
geneviewrs587779043
scholarrs587779043
googlers587779043
pharmgkbrs587779043
gwascentralrs587779043
openSNPrs587779043
23andMers587779043
23andMe allrs587779043
SNP Nexus

SNPshotrs587779043
SNPdbers587779043
MSV3drs587779043
GWAS Ctlgrs587779043
Max Magnitude0
ClinVar
Risk rs587779043(;)
Alt rs587779043(;)
Reference rs587779043(TTCCT;TTCCT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059017_37059021delTCCTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075877.2,