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rs869312770

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs869312770(-;-)
Make rs869312770(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800831
GeneMSH6
is asnp
is mentioned by
dbSNPrs869312770
ebirs869312770
HLIrs869312770
Exacrs869312770
Varsomers869312770
Maprs869312770
PheGenIrs869312770
hapmaprs869312770
1000 genomesrs869312770
hgdprs869312770
ensemblrs869312770
gopubmedrs869312770
geneviewrs869312770
scholarrs869312770
googlers869312770
pharmgkbrs869312770
gwascentralrs869312770
openSNPrs869312770
23andMers869312770
23andMe allrs869312770
SNP Nexus

SNPshotrs869312770
SNPdbers869312770
MSV3drs869312770
GWAS Ctlgrs869312770
Max Magnitude0
ClinVar
Risk rs869312770(;)
Alt rs869312770(;)
Reference rs869312770(AG;AG)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48027970_48027971delAG
CLNSRC
CLNACC RCV000210152.1, RCV000223263.1,