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rs63751594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCTCTTT;TCTCTTT) 0 common in clinvar
(TTTCTCT;TTTCTCT) 0 common in clinvar
Make rs63751594(-;-)
Make rs63751594(-;TCTCTTT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047664
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751594
ebirs63751594
HLIrs63751594
Exacrs63751594
Varsomers63751594
Maprs63751594
PheGenIrs63751594
hapmaprs63751594
1000 genomesrs63751594
hgdprs63751594
ensemblrs63751594
gopubmedrs63751594
geneviewrs63751594
scholarrs63751594
googlers63751594
pharmgkbrs63751594
gwascentralrs63751594
openSNPrs63751594
23andMers63751594
23andMe allrs63751594
SNP Nexus

SNPshotrs63751594
SNPdbers63751594
MSV3drs63751594
GWAS Ctlgrs63751594
Max Magnitude0
ClinVar
Risk rs63751594(;)
Alt rs63751594(;)
Reference rs63751594(TTTCTCT;TTTCTCT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089155_37089161delTCTCTTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075395.2,