rs63750908

Orientation

plus

Stabilized

plus

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

Make rs63750908(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37012054

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750908
dbSNP (classic)	rs63750908
ClinGen	rs63750908
ebi	rs63750908
HLI	rs63750908
Exac	rs63750908
Gnomad	rs63750908
Varsome	rs63750908
LitVar	rs63750908
Map	rs63750908
PheGenI	rs63750908
Biobank	rs63750908
1000 genomes	rs63750908
hgdp	rs63750908
ensembl	rs63750908
geneview	rs63750908
scholar	rs63750908
google	rs63750908
pharmgkb	rs63750908
gwascentral	rs63750908
openSNP	rs63750908
23andMe	rs63750908
SNPshot	rs63750908
SNPdbe	rs63750908
MSV3d	rs63750908
GWAS Ctlg	rs63750908

Max Magnitude

6

ClinVar
Risk	rs63750908(T;T)
Alt	rs63750908(T;T)
Reference	Rs63750908(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37053545_37053546insT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075788.2,