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rs786202328

From SNPedia

Orientationplus
Geno Mag Summary
(ACT;ACT) 0 common in clinvar
Make rs786202328(-;-)
Make rs786202328(-;CTA)
Make rs786202328(CTA;CTA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37000992
GeneMLH1
is asnp
is mentioned by
dbSNPrs786202328
ebirs786202328
HLIrs786202328
Exacrs786202328
Varsomers786202328
Maprs786202328
PheGenIrs786202328
hapmaprs786202328
1000 genomesrs786202328
hgdprs786202328
ensemblrs786202328
gopubmedrs786202328
geneviewrs786202328
scholarrs786202328
googlers786202328
pharmgkbrs786202328
gwascentralrs786202328
openSNPrs786202328
23andMers786202328
23andMe allrs786202328
SNP Nexus

SNPshotrs786202328
SNPdbers786202328
MSV3drs786202328
GWAS Ctlgrs786202328
Max Magnitude0
ClinVar
Risk rs786202328(;)
Alt rs786202328(;)
Reference rs786202328(ACT;ACT)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37042483_37042485delCTA
CLNSRC
CLNACC RCV000165082.1,