rs63749938

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;A)	6	Lynch Syndrome, pathogenic mutation
(A;A)	0	common in clinvar
(I;I)	0

Make rs63749938(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800967

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63749938
dbSNP (classic)	rs63749938
ClinGen	rs63749938
ebi	rs63749938
HLI	rs63749938
Exac	rs63749938
Gnomad	rs63749938
Varsome	rs63749938
LitVar	rs63749938
Map	rs63749938
PheGenI	rs63749938
Biobank	rs63749938
1000 genomes	rs63749938
hgdp	rs63749938
ensembl	rs63749938
geneview	rs63749938
scholar	rs63749938
google	rs63749938
pharmgkb	rs63749938
gwascentral	rs63749938
openSNP	rs63749938
23andMe	rs63749938
SNPshot	rs63749938
SNPdbe	rs63749938
MSV3d	rs63749938
GWAS Ctlg	rs63749938

Max Magnitude

6

ClinVar
Risk	rs63749938(-;-)
Alt	rs63749938(-;-)
Reference	Rs63749938(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028106delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074794.2,