rs587776704

Merged into

rs63751407

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TC)	6	Lynch syndrome, pathogenic mutation
(TC;TC)	0	common in clinvar

Make rs587776704(-;-)

Reference

GRCh38 38.1/142

Chromosome

2

Position

47801036

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587776704
dbSNP (classic)	rs587776704
ClinGen	rs587776704
ebi	rs587776704
HLI	rs587776704
Exac	rs587776704
Gnomad	rs587776704
Varsome	rs587776704
LitVar	rs587776704
Map	rs587776704
PheGenI	rs587776704
Biobank	rs587776704
1000 genomes	rs587776704
hgdp	rs587776704
ensembl	rs587776704
geneview	rs587776704
scholar	rs587776704
google	rs587776704
pharmgkb	rs587776704
gwascentral	rs587776704
openSNP	rs587776704
23andMe	rs587776704
SNPshot	rs587776704
SNPdbe	rs587776704
MSV3d	rs587776704
GWAS Ctlg	rs587776704

Status

Merged into rs63751407

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs587776704(TC;TC)
Significance	Pathogenic
Disease	Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028175_48028176delTC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC	RCV000009489.3, RCV000074799.3,