rs587779287

Orientation

plus

Stabilized

plus

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

Make rs587779287(-;-)

Make rs587779287(GTACATTATTTTC;GTACATTATTTTC)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806282

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779287
dbSNP (classic)	rs587779287
ClinGen	rs587779287
ebi	rs587779287
HLI	rs587779287
Exac	rs587779287
Gnomad	rs587779287
Varsome	rs587779287
LitVar	rs587779287
Map	rs587779287
PheGenI	rs587779287
Biobank	rs587779287
1000 genomes	rs587779287
hgdp	rs587779287
ensembl	rs587779287
geneview	rs587779287
scholar	rs587779287
google	rs587779287
pharmgkb	rs587779287
gwascentral	rs587779287
openSNP	rs587779287
23andMe	rs587779287
SNPshot	rs587779287
SNPdbe	rs587779287
MSV3d	rs587779287
GWAS Ctlg	rs587779287

Max Magnitude

6

ClinVar
Risk	rs587779287(-;-)
Alt	rs587779287(-;-)
Reference	Rs587779287(TCGTACATTATTT;TCGTACATTATTT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033421_48033433delGTACATTATTTTC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074921.2,