rs63749820

Orientation

plus

Stabilized

plus

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

Make rs63749820(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37007046

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749820
dbSNP (classic)	rs63749820
ClinGen	rs63749820
ebi	rs63749820
HLI	rs63749820
Exac	rs63749820
Gnomad	rs63749820
Varsome	rs63749820
LitVar	rs63749820
Map	rs63749820
PheGenI	rs63749820
Biobank	rs63749820
1000 genomes	rs63749820
hgdp	rs63749820
ensembl	rs63749820
geneview	rs63749820
scholar	rs63749820
google	rs63749820
pharmgkb	rs63749820
gwascentral	rs63749820
openSNP	rs63749820
23andMe	rs63749820
SNPshot	rs63749820
SNPdbe	rs63749820
MSV3d	rs63749820
GWAS Ctlg	rs63749820

Max Magnitude

6

ClinVar
Risk	rs63749820(T;T)
Alt	rs63749820(T;T)
Reference	Rs63749820(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37048537C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075706.2,