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rs730881830

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881830(-;-)
Make rs730881830(-;TC)
Make rs730881830(TC;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806590
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs730881830
ebirs730881830
HLIrs730881830
Exacrs730881830
Varsomers730881830
Maprs730881830
PheGenIrs730881830
hapmaprs730881830
1000 genomesrs730881830
hgdprs730881830
ensemblrs730881830
gopubmedrs730881830
geneviewrs730881830
scholarrs730881830
googlers730881830
pharmgkbrs730881830
gwascentralrs730881830
openSNPrs730881830
23andMers730881830
23andMe allrs730881830
SNP Nexus

SNPshotrs730881830
SNPdbers730881830
MSV3drs730881830
GWAS Ctlgrs730881830
Max Magnitude0
ClinVar
Risk rs730881830(TC;TC)
Alt rs730881830(TC;TC)
Reference rs730881830(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FBXO11 MSH6
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48033728_48033729dupTC
CLNSRC
CLNACC RCV000160746.1, RCV000213532.1,