rs63750677

Orientation

plus

Stabilized

plus

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

Make rs63750677(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020436

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750677
dbSNP (classic)	rs63750677
ClinGen	rs63750677
ebi	rs63750677
HLI	rs63750677
Exac	rs63750677
Gnomad	rs63750677
Varsome	rs63750677
LitVar	rs63750677
Map	rs63750677
PheGenI	rs63750677
Biobank	rs63750677
1000 genomes	rs63750677
hgdp	rs63750677
ensembl	rs63750677
geneview	rs63750677
scholar	rs63750677
google	rs63750677
pharmgkb	rs63750677
gwascentral	rs63750677
openSNP	rs63750677
23andMe	rs63750677
SNPshot	rs63750677
SNPdbe	rs63750677
MSV3d	rs63750677
GWAS Ctlg	rs63750677

Max Magnitude

6

ClinVar
Risk	rs63750677(C;C)
Alt	rs63750677(C;C)
Reference	Rs63750677(-;-)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37061927dupC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075073.3, RCV000478965.1,