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rs786202767

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786202767(-;-)
Make rs786202767(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37050544
GeneMLH1
is asnp
is mentioned by
dbSNPrs786202767
ebirs786202767
HLIrs786202767
Exacrs786202767
Varsomers786202767
Maprs786202767
PheGenIrs786202767
hapmaprs786202767
1000 genomesrs786202767
hgdprs786202767
ensemblrs786202767
gopubmedrs786202767
geneviewrs786202767
scholarrs786202767
googlers786202767
pharmgkbrs786202767
gwascentralrs786202767
openSNPrs786202767
23andMers786202767
23andMe allrs786202767
SNP Nexus

SNPshotrs786202767
SNPdbers786202767
MSV3drs786202767
GWAS Ctlgrs786202767
Max Magnitude0
ClinVar
Risk rs786202767(;)
Alt rs786202767(;)
Reference rs786202767(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37092035delA
CLNSRC
CLNACC RCV000165746.1,