rs63750036

Orientation

plus

Stabilized

plus

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

Make rs63750036(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37040247

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750036
dbSNP (classic)	rs63750036
ClinGen	rs63750036
ebi	rs63750036
HLI	rs63750036
Exac	rs63750036
Gnomad	rs63750036
Varsome	rs63750036
LitVar	rs63750036
Map	rs63750036
PheGenI	rs63750036
Biobank	rs63750036
1000 genomes	rs63750036
hgdp	rs63750036
ensembl	rs63750036
geneview	rs63750036
scholar	rs63750036
google	rs63750036
pharmgkb	rs63750036
gwascentral	rs63750036
openSNP	rs63750036
23andMe	rs63750036
SNPshot	rs63750036
SNPdbe	rs63750036
MSV3d	rs63750036
GWAS Ctlg	rs63750036

Max Magnitude

6

ClinVar
Risk	rs63750036(-;-)
Alt	rs63750036(-;-)
Reference	Rs63750036(GG;GG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37081738_37081739delGG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075281.2,