rs63749818

Orientation

plus

Stabilized

plus

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

Make rs63749818(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37007002

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749818
dbSNP (classic)	rs63749818
ClinGen	rs63749818
ebi	rs63749818
HLI	rs63749818
Exac	rs63749818
Gnomad	rs63749818
Varsome	rs63749818
LitVar	rs63749818
Map	rs63749818
PheGenI	rs63749818
Biobank	rs63749818
1000 genomes	rs63749818
hgdp	rs63749818
ensembl	rs63749818
geneview	rs63749818
scholar	rs63749818
google	rs63749818
pharmgkb	rs63749818
gwascentral	rs63749818
openSNP	rs63749818
23andMe	rs63749818
SNPshot	rs63749818
SNPdbe	rs63749818
MSV3d	rs63749818
GWAS Ctlg	rs63749818

Max Magnitude

6

ClinVar
Risk	rs63749818(A;A) rs63749818(G;G)
Alt	rs63749818(A;A) rs63749818(G;G)
Reference	Rs63749818(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37048493C>A; NC_000003.11:g.37048493C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075696.2, RCV000220277.1,