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rs752514155

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752514155(A;A)
Make rs752514155(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position214809515
GeneBARD1, LOC101928103
is asnp
is mentioned by
dbSNPrs752514155
ebirs752514155
HLIrs752514155
Exacrs752514155
Varsomers752514155
Maprs752514155
PheGenIrs752514155
hapmaprs752514155
1000 genomesrs752514155
hgdprs752514155
ensemblrs752514155
gopubmedrs752514155
geneviewrs752514155
scholarrs752514155
googlers752514155
pharmgkbrs752514155
gwascentralrs752514155
openSNPrs752514155
23andMers752514155
23andMe allrs752514155
SNP Nexus

SNPshotrs752514155
SNPdbers752514155
MSV3drs752514155
GWAS Ctlgrs752514155
Max Magnitude0
ClinVar
Risk rs752514155(A;A)
Alt rs752514155(A;A)
Reference rs752514155(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene LOC101928103 BARD1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.215674239C>A
CLNSRC
CLNACC RCV000215389.1,