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rs786203244

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TGAGTCAAAAATGTTT) 3 2-4 fold higher risk for breast cancer, depending on family history
(TGAGTCAAAAATGTTT;TGAGTCAAAAATGTTT) 0 common in clinvar
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position23630225
GenePALB2
is asnp
is mentioned by
dbSNPrs786203244
ebirs786203244
HLIrs786203244
Exacrs786203244
Varsomers786203244
Maprs786203244
PheGenIrs786203244
hapmaprs786203244
1000 genomesrs786203244
hgdprs786203244
ensemblrs786203244
gopubmedrs786203244
geneviewrs786203244
scholarrs786203244
googlers786203244
pharmgkbrs786203244
gwascentralrs786203244
openSNPrs786203244
23andMers786203244
23andMe allrs786203244
SNP Nexus

SNPshotrs786203244
SNPdbers786203244
MSV3drs786203244
GWAS Ctlgrs786203244
Max Magnitude7
ClinVar
Risk rs786203244(;)
Alt rs786203244(;)
Reference rs786203244(TGAGTCAAAAATGTTT;TGAGTCAAAAATGTTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PALB2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000016.9:g.23641546_23641561del16
CLNSRC
CLNACC RCV000166469.1,