rs121434628

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121434628(C;T)

Make rs121434628(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

189844078

Gene

PMS1

is a	snp
is	mentioned by
dbSNP	rs121434628
dbSNP (classic)	rs121434628
ClinGen	rs121434628
ebi	rs121434628
HLI	rs121434628
Exac	rs121434628
Gnomad	rs121434628
Varsome	rs121434628
LitVar	rs121434628
Map	rs121434628
PheGenI	rs121434628
Biobank	rs121434628
1000 genomes	rs121434628
hgdp	rs121434628
ensembl	rs121434628
geneview	rs121434628
scholar	rs121434628
google	rs121434628
pharmgkb	rs121434628
gwascentral	rs121434628
openSNP	rs121434628
23andMe	rs121434628
SNPshot	rs121434628
SNPdbe	rs121434628
MSV3d	rs121434628
GWAS Ctlg	rs121434628

Max Magnitude

0

OMIM	600258
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434628(T;T)
Alt	rs121434628(T;T)
Reference	Rs121434628(C;C)
Significance	Untested
Disease	Hereditary nonpolyposis colorectal cancer type 3
Variation	info
Gene	PMS1
CLNDBN	Hereditary nonpolyposis colorectal cancer type 3
Reversed	0
HGVS	NC_000002.11:g.190708804C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000030052.1,