rs63749950

Orientation

plus

Stabilized

plus

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

Make rs63749950(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017557

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749950
dbSNP (classic)	rs63749950
ClinGen	rs63749950
ebi	rs63749950
HLI	rs63749950
Exac	rs63749950
Gnomad	rs63749950
Varsome	rs63749950
LitVar	rs63749950
Map	rs63749950
PheGenI	rs63749950
Biobank	rs63749950
1000 genomes	rs63749950
hgdp	rs63749950
ensembl	rs63749950
geneview	rs63749950
scholar	rs63749950
google	rs63749950
pharmgkb	rs63749950
gwascentral	rs63749950
openSNP	rs63749950
23andMe	rs63749950
SNPshot	rs63749950
SNPdbe	rs63749950
MSV3d	rs63749950
GWAS Ctlg	rs63749950

Max Magnitude

6

ClinVar
Risk	rs63749950(T;T)
Alt	rs63749950(T;T)
Reference	Rs63749950(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059048C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075883.2,