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rs587778958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587778958(-;GATTACCCCTTCTG)
Make rs587778958(GATTACCCCTTCTG;GATTACCCCTTCTG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048546
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778958
dbSNP (old)rs587778958
ClinGenrs587778958
ebirs587778958
HLIrs587778958
Exacrs587778958
Gnomadrs587778958
Varsomers587778958
Maprs587778958
PheGenIrs587778958
Biobankrs587778958
1000 genomesrs587778958
hgdprs587778958
ensemblrs587778958
gopubmedrs587778958
geneviewrs587778958
scholarrs587778958
googlers587778958
pharmgkbrs587778958
gwascentralrs587778958
openSNPrs587778958
23andMers587778958
23andMe allrs587778958
SNP Nexus

SNPshotrs587778958
SNPdbers587778958
MSV3drs587778958
GWAS Ctlgrs587778958
Max Magnitude0
ClinVar
Risk rs587778958(TGGATTACCCCTTC;TGGATTACCCCTTC)
Alt rs587778958(TGGATTACCCCTTC;TGGATTACCCCTTC)
Reference Rs587778958(-;-)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37090024_37090037dupGATTACCCCTTCTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075421.2, RCV000202103.1,