rs1057515572

Orientation

minus

Stabilized

minus

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

Make rs1057515572(AGT;AGT)

Make rs1057515572(AGT;GC)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

5987033

Gene

PMS2

is a	snp
is	mentioned by
dbSNP	rs1057515572
dbSNP (classic)	rs1057515572
ClinGen	rs1057515572
ebi	rs1057515572
HLI	rs1057515572
Exac	rs1057515572
Gnomad	rs1057515572
Varsome	rs1057515572
LitVar	rs1057515572
Map	rs1057515572
PheGenI	rs1057515572
Biobank	rs1057515572
1000 genomes	rs1057515572
hgdp	rs1057515572
ensembl	rs1057515572
geneview	rs1057515572
scholar	rs1057515572
google	rs1057515572
pharmgkb	rs1057515572
gwascentral	rs1057515572
openSNP	rs1057515572
23andMe	rs1057515572
SNPshot	rs1057515572
SNPdbe	rs1057515572
MSV3d	rs1057515572
GWAS Ctlg	rs1057515572

Max Magnitude

0

ClinVar
Risk	rs1057515572(AGT;AGT)
Alt	rs1057515572(AGT;AGT)
Reference	Rs1057515572(GC;GC)
Significance	Pathogenic
Disease	Turcot syndrome
Variation	info
Gene	PMS2
CLNDBN	Turcot syndrome
Reversed	1
HGVS	NC_000007.13:g.6026664_6026665delGCinsACT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009825.3,