rs63750962

Orientation

plus

Stabilized

plus

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

Make rs63750962(GC;GC)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020347

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750962
dbSNP (classic)	rs63750962
ClinGen	rs63750962
ebi	rs63750962
HLI	rs63750962
Exac	rs63750962
Gnomad	rs63750962
Varsome	rs63750962
LitVar	rs63750962
Map	rs63750962
PheGenI	rs63750962
Biobank	rs63750962
1000 genomes	rs63750962
hgdp	rs63750962
ensembl	rs63750962
geneview	rs63750962
scholar	rs63750962
google	rs63750962
pharmgkb	rs63750962
gwascentral	rs63750962
openSNP	rs63750962
23andMe	rs63750962
SNPshot	rs63750962
SNPdbe	rs63750962
MSV3d	rs63750962
GWAS Ctlg	rs63750962

Max Magnitude

6

ClinVar
Risk	rs63750962(GC;GC)
Alt	rs63750962(GC;GC)
Reference	Rs63750962(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061837_37061838dupGC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075936.2,