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rs149364097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149364097(C;G)
Make rs149364097(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position61801348
GeneBRIP1
is asnp
is mentioned by
dbSNPrs149364097
ebirs149364097
HLIrs149364097
Exacrs149364097
Varsomers149364097
Maprs149364097
PheGenIrs149364097
hapmaprs149364097
1000 genomesrs149364097
hgdprs149364097
ensemblrs149364097
gopubmedrs149364097
geneviewrs149364097
scholarrs149364097
googlers149364097
pharmgkbrs149364097
gwascentralrs149364097
openSNPrs149364097
23andMers149364097
23andMe allrs149364097
SNP Nexus

SNPshotrs149364097
SNPdbers149364097
MSV3drs149364097
GWAS Ctlgrs149364097
Max Magnitude0
ClinVar
Risk rs149364097(G;G)
Alt rs149364097(G;G)
Reference rs149364097(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Fanconi anemia not specified Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRIP1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Fanconi anemia, complementation group J not specified Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000017.10:g.59878709C>A; NC_000017.10:g.59878709C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000213526.1, RCV000023492.2, RCV000120412.1, RCV000131544.2, RCV000216316.1,