rs121908291

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs121908291(C;T)

Make rs121908291(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

168878306

Gene

PALLD

is a	snp
is	mentioned by
dbSNP	rs121908291
dbSNP (classic)	rs121908291
ClinGen	rs121908291
ebi	rs121908291
HLI	rs121908291
Exac	rs121908291
Gnomad	rs121908291
Varsome	rs121908291
LitVar	rs121908291
Map	rs121908291
PheGenI	rs121908291
Biobank	rs121908291
1000 genomes	rs121908291
hgdp	rs121908291
ensembl	rs121908291
geneview	rs121908291
scholar	rs121908291
google	rs121908291
pharmgkb	rs121908291
gwascentral	rs121908291
openSNP	rs121908291
23andMe	rs121908291
SNPshot	rs121908291
SNPdbe	rs121908291
MSV3d	rs121908291
GWAS Ctlg	rs121908291

Max Magnitude

0

OMIM	608092
Desc
Variant	0001
Related	also

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, RCV000168440.5,