rs63750212

Orientation

plus

Stabilized

plus

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

Make rs63750212(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017571

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750212
dbSNP (classic)	rs63750212
ClinGen	rs63750212
ebi	rs63750212
HLI	rs63750212
Exac	rs63750212
Gnomad	rs63750212
Varsome	rs63750212
LitVar	rs63750212
Map	rs63750212
PheGenI	rs63750212
Biobank	rs63750212
1000 genomes	rs63750212
hgdp	rs63750212
ensembl	rs63750212
geneview	rs63750212
scholar	rs63750212
google	rs63750212
pharmgkb	rs63750212
gwascentral	rs63750212
openSNP	rs63750212
23andMe	rs63750212
SNPshot	rs63750212
SNPdbe	rs63750212
MSV3d	rs63750212
GWAS Ctlg	rs63750212

Max Magnitude

6

ClinVar
Risk	rs63750212(T;T)
Alt	rs63750212(T;T)
Reference	Rs63750212(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059062_37059063insT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075888.2,