rs267608042

Orientation

plus

Stabilized

plus

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

Make rs267608042(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47801102

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608042
dbSNP (classic)	rs267608042
ClinGen	rs267608042
ebi	rs267608042
HLI	rs267608042
Exac	rs267608042
Gnomad	rs267608042
Varsome	rs267608042
LitVar	rs267608042
Map	rs267608042
PheGenI	rs267608042
Biobank	rs267608042
1000 genomes	rs267608042
hgdp	rs267608042
ensembl	rs267608042
geneview	rs267608042
scholar	rs267608042
google	rs267608042
pharmgkb	rs267608042
gwascentral	rs267608042
openSNP	rs267608042
23andMe	rs267608042
SNPshot	rs267608042
SNPdbe	rs267608042
MSV3d	rs267608042
GWAS Ctlg	rs267608042

Max Magnitude

6

ClinVar
Risk	rs267608042(-;-)
Alt	rs267608042(-;-)
Reference	Rs267608042(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48028241_48028242delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074804.2, RCV000486939.1, RCV000491377.1,