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rs886037989

From SNPedia

Merged intors80357632
Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAT;AAAT) 0 common in clinvar
Make rs886037989(-;-)
Make rs886037989(-;AAAT)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position43094027
GeneBRCA1
is asnp
is mentioned by
dbSNPrs886037989
dbSNP (classic)rs886037989
ClinGenrs886037989
ebirs886037989
HLIrs886037989
Exacrs886037989
Gnomadrs886037989
Varsomers886037989
LitVarrs886037989
Maprs886037989
PheGenIrs886037989
Biobankrs886037989
1000 genomesrs886037989
hgdprs886037989
ensemblrs886037989
geneviewrs886037989
scholarrs886037989
googlers886037989
pharmgkbrs886037989
gwascentralrs886037989
openSNPrs886037989
23andMers886037989
SNPshotrs886037989
SNPdbers886037989
MSV3drs886037989
GWAS Ctlgrs886037989
StatusMerged into rs80357632
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs886037989(AAAT;AAAT)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41246044_41246047delATTT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047496.2, RCV000241074.2,