rs587783056

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TT)	6	Lynch syndrome
(I;I)	0	common genotype
(TT;TT)	0	common in clinvar

Make rs587783056(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47799688

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587783056
dbSNP (classic)	rs587783056
ClinGen	rs587783056
ebi	rs587783056
HLI	rs587783056
Exac	rs587783056
Gnomad	rs587783056
Varsome	rs587783056
LitVar	rs587783056
Map	rs587783056
PheGenI	rs587783056
Biobank	rs587783056
1000 genomes	rs587783056
hgdp	rs587783056
ensembl	rs587783056
geneview	rs587783056
scholar	rs587783056
google	rs587783056
pharmgkb	rs587783056
gwascentral	rs587783056
openSNP	rs587783056
23andMe	rs587783056
SNPshot	rs587783056
SNPdbe	rs587783056
MSV3d	rs587783056
GWAS Ctlg	rs587783056

Max Magnitude

6

ClinVar
Risk	rs587783056(-;-)
Alt	rs587783056(-;-)
Reference	Rs587783056(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026827_48026828delTT
CLNSRC
CLNACC	RCV000144627.1, RCV000216742.1,