rs63750736

Orientation

plus

Stabilized

plus

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

Make rs63750736(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020314

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750736
dbSNP (classic)	rs63750736
ClinGen	rs63750736
ebi	rs63750736
HLI	rs63750736
Exac	rs63750736
Gnomad	rs63750736
Varsome	rs63750736
LitVar	rs63750736
Map	rs63750736
PheGenI	rs63750736
Biobank	rs63750736
1000 genomes	rs63750736
hgdp	rs63750736
ensembl	rs63750736
geneview	rs63750736
scholar	rs63750736
google	rs63750736
pharmgkb	rs63750736
gwascentral	rs63750736
openSNP	rs63750736
23andMe	rs63750736
SNPshot	rs63750736
SNPdbe	rs63750736
MSV3d	rs63750736
GWAS Ctlg	rs63750736

Max Magnitude

6

ClinVar
Risk	rs63750736(A;A) rs63750736(T;T)
Alt	rs63750736(A;A) rs63750736(T;T)
Reference	Rs63750736(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061805G>A; NC_000003.11:g.37061805G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075926.2, RCV000075927.2,