rs63750561

Orientation

plus

Stabilized

plus

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

Make rs63750561(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050517

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750561
dbSNP (classic)	rs63750561
ClinGen	rs63750561
ebi	rs63750561
HLI	rs63750561
Exac	rs63750561
Gnomad	rs63750561
Varsome	rs63750561
LitVar	rs63750561
Map	rs63750561
PheGenI	rs63750561
Biobank	rs63750561
1000 genomes	rs63750561
hgdp	rs63750561
ensembl	rs63750561
geneview	rs63750561
scholar	rs63750561
google	rs63750561
pharmgkb	rs63750561
gwascentral	rs63750561
openSNP	rs63750561
23andMe	rs63750561
SNPshot	rs63750561
SNPdbe	rs63750561
MSV3d	rs63750561
GWAS Ctlg	rs63750561

Max Magnitude

6

ClinVar
Risk	rs63750561(A;A) rs63750561(T;T)
Alt	rs63750561(A;A) rs63750561(T;T)
Reference	Rs63750561(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37092008G>A; NC_000003.11:g.37092008G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075550.2, RCV000202047.1, RCV000468327.1,