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rs786202008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;TCCCTGTGCCAAAGAGA) 3 2-4 fold higher risk for breast cancer, depending on family history
(TCCCTGTGCCAAAGAGA;TCCCTGTGCCAAAGAGA) 7 Fanconi anemia, complementation group N


Make rs786202008(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23607969
GenePALB2
is asnp
is mentioned by
dbSNPrs786202008
ebirs786202008
HLIrs786202008
Exacrs786202008
Varsomers786202008
Maprs786202008
PheGenIrs786202008
hapmaprs786202008
1000 genomesrs786202008
hgdprs786202008
ensemblrs786202008
gopubmedrs786202008
geneviewrs786202008
scholarrs786202008
googlers786202008
pharmgkbrs786202008
gwascentralrs786202008
openSNPrs786202008
23andMers786202008
23andMe allrs786202008
SNP Nexus

SNPshotrs786202008
SNPdbers786202008
MSV3drs786202008
GWAS Ctlgrs786202008
Max Magnitude7
ClinVar
Risk rs786202008(TCCCTGTGCCAAAGAGA;TCCCTGTGCCAAAGAGA)
Alt rs786202008(TCCCTGTGCCAAAGAGA;TCCCTGTGCCAAAGAGA)
Reference rs786202008(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23619291_23619307dup17
CLNSRC
CLNACC RCV000164597.1,