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rs786202336

From SNPedia

Orientationplus
Geno Mag Summary
(AGTGG;AGTGG) 0 common in clinvar
Make rs786202336(-;-)
Make rs786202336(-;TGGAG)
Make rs786202336(TGGAG;TGGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799042
GeneMSH6
is asnp
is mentioned by
dbSNPrs786202336
ebirs786202336
HLIrs786202336
Exacrs786202336
Varsomers786202336
Maprs786202336
PheGenIrs786202336
hapmaprs786202336
1000 genomesrs786202336
hgdprs786202336
ensemblrs786202336
gopubmedrs786202336
geneviewrs786202336
scholarrs786202336
googlers786202336
pharmgkbrs786202336
gwascentralrs786202336
openSNPrs786202336
23andMers786202336
23andMe allrs786202336
SNP Nexus

SNPshotrs786202336
SNPdbers786202336
MSV3drs786202336
GWAS Ctlgrs786202336
Max Magnitude0
ClinVar
Risk rs786202336(;)
Alt rs786202336(;)
Reference rs786202336(AGTGG;AGTGG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026181_48026185delTGGAG
CLNSRC
CLNACC RCV000165096.1,