rs63750035

Orientation

plus

Stabilized

plus

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

Make rs63750035(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047570

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750035
dbSNP (classic)	rs63750035
ClinGen	rs63750035
ebi	rs63750035
HLI	rs63750035
Exac	rs63750035
Gnomad	rs63750035
Varsome	rs63750035
LitVar	rs63750035
Map	rs63750035
PheGenI	rs63750035
Biobank	rs63750035
1000 genomes	rs63750035
hgdp	rs63750035
ensembl	rs63750035
geneview	rs63750035
scholar	rs63750035
google	rs63750035
pharmgkb	rs63750035
gwascentral	rs63750035
openSNP	rs63750035
23andMe	rs63750035
SNPshot	rs63750035
SNPdbe	rs63750035
MSV3d	rs63750035
GWAS Ctlg	rs63750035

Max Magnitude

6

ClinVar
Risk	rs63750035(-;-)
Alt	rs63750035(-;-)
Reference	Rs63750035(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089061_37089062delAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075364.2,