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rs749602688

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs749602688(A;A)
Make rs749602688(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23630088
GenePALB2
is asnp
is mentioned by
dbSNPrs749602688
ebirs749602688
HLIrs749602688
Exacrs749602688
Varsomers749602688
Maprs749602688
PheGenIrs749602688
hapmaprs749602688
1000 genomesrs749602688
hgdprs749602688
ensemblrs749602688
gopubmedrs749602688
geneviewrs749602688
scholarrs749602688
googlers749602688
pharmgkbrs749602688
gwascentralrs749602688
openSNPrs749602688
23andMers749602688
23andMe allrs749602688
SNP Nexus

SNPshotrs749602688
SNPdbers749602688
MSV3drs749602688
GWAS Ctlgrs749602688
Max Magnitude0
ClinVar
Risk rs749602688(A;A)
Alt rs749602688(A;A)
Reference rs749602688(G;G)
Significance Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided
Reversed 0
HGVS NC_000016.9:g.23641409G>A; NC_000016.9:g.23641409G>T
CLNSRC
CLNACC RCV000228021.1, RCV000236381.1,