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rs876658864

From SNPedia

Orientationplus
Geno Mag Summary
(TGGCCCT;TGGCCCT) 0 common in clinvar
Make rs876658864(GG;GG)
Make rs876658864(GG;TGGCCCT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800019
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658864
ebirs876658864
HLIrs876658864
Exacrs876658864
Varsomers876658864
Maprs876658864
PheGenIrs876658864
hapmaprs876658864
1000 genomesrs876658864
hgdprs876658864
ensemblrs876658864
gopubmedrs876658864
geneviewrs876658864
scholarrs876658864
googlers876658864
pharmgkbrs876658864
gwascentralrs876658864
openSNPrs876658864
23andMers876658864
23andMe allrs876658864
SNP Nexus

SNPshotrs876658864
SNPdbers876658864
MSV3drs876658864
GWAS Ctlgrs876658864
Max Magnitude0
ClinVar
Risk rs876658864(GG;GG)
Alt rs876658864(GG;GG)
Reference rs876658864(TGGCCCT;TGGCCCT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48027158_48027164delTGGCCCTinsGG
CLNSRC
CLNACC RCV000219907.1,