rs63749874

Orientation

plus

Stabilized

plus

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

Make rs63749874(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799617

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63749874
dbSNP (classic)	rs63749874
ClinGen	rs63749874
ebi	rs63749874
HLI	rs63749874
Exac	rs63749874
Gnomad	rs63749874
Varsome	rs63749874
LitVar	rs63749874
Map	rs63749874
PheGenI	rs63749874
Biobank	rs63749874
1000 genomes	rs63749874
hgdp	rs63749874
ensembl	rs63749874
geneview	rs63749874
scholar	rs63749874
google	rs63749874
pharmgkb	rs63749874
gwascentral	rs63749874
openSNP	rs63749874
23andMe	rs63749874
SNPshot	rs63749874
SNPdbe	rs63749874
MSV3d	rs63749874
GWAS Ctlg	rs63749874

Max Magnitude

6

ClinVar
Risk	rs63749874(-;-)
Alt	rs63749874(-;-)
Reference	Rs63749874(AAAG;AAAG)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026756_48026759delAAGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074674.2, RCV000115378.5,