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rs876660630

From SNPedia

Orientationplus
Geno Mag Summary
(TTAAGTCTA;TTAAGTCTA) 0 common in clinvar
Make rs876660630(-;-)
Make rs876660630(-;TTAAGTCTA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800628
GeneMSH6
is asnp
is mentioned by
dbSNPrs876660630
ebirs876660630
HLIrs876660630
Exacrs876660630
Varsomers876660630
Maprs876660630
PheGenIrs876660630
hapmaprs876660630
1000 genomesrs876660630
hgdprs876660630
ensemblrs876660630
gopubmedrs876660630
geneviewrs876660630
scholarrs876660630
googlers876660630
pharmgkbrs876660630
gwascentralrs876660630
openSNPrs876660630
23andMers876660630
23andMe allrs876660630
SNP Nexus

SNPshotrs876660630
SNPdbers876660630
MSV3drs876660630
GWAS Ctlgrs876660630
Max Magnitude0
ClinVar
Risk rs876660630(;)
Alt rs876660630(;)
Reference rs876660630(TTAAGTCTA;TTAAGTCTA)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Variation info
Gene MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027767_48027775delTTAAGTCTA
CLNSRC
CLNACC RCV000217977.1, RCV000229744.1,