rs63749956

Orientation

plus

Stabilized

plus

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

Make rs63749956(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996652

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749956
dbSNP (classic)	rs63749956
ClinGen	rs63749956
ebi	rs63749956
HLI	rs63749956
Exac	rs63749956
Gnomad	rs63749956
Varsome	rs63749956
LitVar	rs63749956
Map	rs63749956
PheGenI	rs63749956
Biobank	rs63749956
1000 genomes	rs63749956
hgdp	rs63749956
ensembl	rs63749956
geneview	rs63749956
scholar	rs63749956
google	rs63749956
pharmgkb	rs63749956
gwascentral	rs63749956
openSNP	rs63749956
23andMe	rs63749956
SNPshot	rs63749956
SNPdbe	rs63749956
MSV3d	rs63749956
GWAS Ctlg	rs63749956

Max Magnitude

6

ClinVar
Risk	rs63749956(T;T)
Alt	rs63749956(T;T)
Reference	Rs63749956(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038143dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075230.2,