rs587781362

Merged into

rs63749942

Orientation

plus

Stabilized

plus

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

Make rs587781362(-;-)

Make rs587781362(-;GTC)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806279

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587781362
dbSNP (classic)	rs587781362
ClinGen	rs587781362
ebi	rs587781362
HLI	rs587781362
Exac	rs587781362
Gnomad	rs587781362
Varsome	rs587781362
LitVar	rs587781362
Map	rs587781362
PheGenI	rs587781362
Biobank	rs587781362
1000 genomes	rs587781362
hgdp	rs587781362
ensembl	rs587781362
geneview	rs587781362
scholar	rs587781362
google	rs587781362
pharmgkb	rs587781362
gwascentral	rs587781362
openSNP	rs587781362
23andMe	rs587781362
SNPshot	rs587781362
SNPdbe	rs587781362
MSV3d	rs587781362
GWAS Ctlg	rs587781362

Status

Merged into rs63749942

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs587781362(GTC;GTC)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48033420_48033422delCGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074918.2, RCV000129144.3, RCV000255857.1,