rs751415161

Merged into

rs587776424

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23603591

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs751415161
dbSNP (classic)	rs751415161
ClinGen	rs751415161
ebi	rs751415161
HLI	rs751415161
Exac	rs751415161
Gnomad	rs751415161
Varsome	rs751415161
LitVar	rs751415161
Map	rs751415161
PheGenI	rs751415161
Biobank	rs751415161
1000 genomes	rs751415161
hgdp	rs751415161
ensembl	rs751415161
geneview	rs751415161
scholar	rs751415161
google	rs751415161
pharmgkb	rs751415161
gwascentral	rs751415161
openSNP	rs751415161
23andMe	rs751415161
SNPshot	rs751415161
SNPdbe	rs751415161
MSV3d	rs751415161
GWAS Ctlg	rs751415161

Status

Merged into rs587776424

Max Magnitude

7

ClinVar
Risk
Alt
Reference	Rs751415161(AAGT;AAGT)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.23614912_23614915delAAGT
CLNSRC
CLNACC	RCV000133486.1, RCV000165289.2,