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rs121908291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121908291(C;T)
Make rs121908291(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position168878306
GenePALLD
is asnp
is mentioned by
dbSNPrs121908291
ebirs121908291
HLIrs121908291
Exacrs121908291
Varsomers121908291
Maprs121908291
PheGenIrs121908291
hapmaprs121908291
1000 genomesrs121908291
hgdprs121908291
ensemblrs121908291
gopubmedrs121908291
geneviewrs121908291
scholarrs121908291
googlers121908291
pharmgkbrs121908291
gwascentralrs121908291
openSNPrs121908291
23andMers121908291
23andMe allrs121908291
SNP Nexus

SNPshotrs121908291
SNPdbers121908291
MSV3drs121908291
GWAS Ctlgrs121908291
Max Magnitude0
OMIM608092
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908291(T;T)
Alt rs121908291(T;T)
Reference rs121908291(C;C)
Significance Other
Disease Pancreatic cancer 1 not specified Pancreatic adenocarcinoma
Variation info
Gene PALLD
CLNDBN Pancreatic cancer 1 not specified Pancreatic adenocarcinoma
Reversed 0
HGVS NC_000004.11:g.169799457C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002681.2, RCV000160876.1, RCV000168440.4,