rs1057517551

Orientation

plus

Stabilized

plus

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

Make rs1057517551(-;T)

Make rs1057517551(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47798891

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1057517551
dbSNP (classic)	rs1057517551
ClinGen	rs1057517551
ebi	rs1057517551
HLI	rs1057517551
Exac	rs1057517551
Gnomad	rs1057517551
Varsome	rs1057517551
LitVar	rs1057517551
Map	rs1057517551
PheGenI	rs1057517551
Biobank	rs1057517551
1000 genomes	rs1057517551
hgdp	rs1057517551
ensembl	rs1057517551
geneview	rs1057517551
scholar	rs1057517551
google	rs1057517551
pharmgkb	rs1057517551
gwascentral	rs1057517551
openSNP	rs1057517551
23andMe	rs1057517551
SNPshot	rs1057517551
SNPdbe	rs1057517551
MSV3d	rs1057517551
GWAS Ctlg	rs1057517551

Max Magnitude

0

ClinVar
Risk	rs1057517551(T;T)
Alt	rs1057517551(T;T)
Reference	Rs1057517551(-;-)
Significance	Pathogenic
Disease	Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026030dupT
CLNSRC
CLNACC	RCV000411044.1, RCV000473148.1, RCV000482391.1, RCV000491372.1,