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rs746604683

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746604683(A;A)
Make rs746604683(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626390
GenePALB2
is asnp
is mentioned by
dbSNPrs746604683
ebirs746604683
HLIrs746604683
Exacrs746604683
Varsomers746604683
Maprs746604683
PheGenIrs746604683
hapmaprs746604683
1000 genomesrs746604683
hgdprs746604683
ensemblrs746604683
gopubmedrs746604683
geneviewrs746604683
scholarrs746604683
googlers746604683
pharmgkbrs746604683
gwascentralrs746604683
openSNPrs746604683
23andMers746604683
23andMe allrs746604683
SNP Nexus

SNPshotrs746604683
SNPdbers746604683
MSV3drs746604683
GWAS Ctlgrs746604683
Max Magnitude0
ClinVar
Risk rs746604683(A;A)
Alt rs746604683(A;A)
Reference rs746604683(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000016.9:g.23637711G>C
CLNSRC
CLNACC RCV000234617.1,