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rs786204317

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204317(-;-)
Make rs786204317(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37020401
GeneMLH1
is asnp
is mentioned by
dbSNPrs786204317
ebirs786204317
HLIrs786204317
Exacrs786204317
Varsomers786204317
Maprs786204317
PheGenIrs786204317
hapmaprs786204317
1000 genomesrs786204317
hgdprs786204317
ensemblrs786204317
gopubmedrs786204317
geneviewrs786204317
scholarrs786204317
googlers786204317
pharmgkbrs786204317
gwascentralrs786204317
openSNPrs786204317
23andMers786204317
23andMe allrs786204317
SNP Nexus

SNPshotrs786204317
SNPdbers786204317
MSV3drs786204317
GWAS Ctlgrs786204317
Max Magnitude0
ClinVar
Risk rs786204317(;)
Alt rs786204317(;)
Reference rs786204317(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061892delG
CLNSRC
CLNACC RCV000168718.1,