rs63750281

Orientation

plus

Stabilized

plus

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

Make rs63750281(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996705

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750281
dbSNP (classic)	rs63750281
ClinGen	rs63750281
ebi	rs63750281
HLI	rs63750281
Exac	rs63750281
Gnomad	rs63750281
Varsome	rs63750281
LitVar	rs63750281
Map	rs63750281
PheGenI	rs63750281
Biobank	rs63750281
1000 genomes	rs63750281
hgdp	rs63750281
ensembl	rs63750281
geneview	rs63750281
scholar	rs63750281
google	rs63750281
pharmgkb	rs63750281
gwascentral	rs63750281
openSNP	rs63750281
23andMe	rs63750281
SNPshot	rs63750281
SNPdbe	rs63750281
MSV3d	rs63750281
GWAS Ctlg	rs63750281

Max Magnitude

6

ClinVar
Risk	rs63750281(A;A)
Alt	rs63750281(A;A)
Reference	Rs63750281(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038196T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075492.2,