rs63751415

Orientation

plus

Stabilized

plus

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

Make rs63751415(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047662

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751415
dbSNP (classic)	rs63751415
ClinGen	rs63751415
ebi	rs63751415
HLI	rs63751415
Exac	rs63751415
Gnomad	rs63751415
Varsome	rs63751415
LitVar	rs63751415
Map	rs63751415
PheGenI	rs63751415
Biobank	rs63751415
1000 genomes	rs63751415
hgdp	rs63751415
ensembl	rs63751415
geneview	rs63751415
scholar	rs63751415
google	rs63751415
pharmgkb	rs63751415
gwascentral	rs63751415
openSNP	rs63751415
23andMe	rs63751415
SNPshot	rs63751415
SNPdbe	rs63751415
MSV3d	rs63751415
GWAS Ctlg	rs63751415

Max Magnitude

6

ClinVar
Risk	rs63751415(G;G)
Alt	rs63751415(G;G)
Reference	Rs63751415(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089153T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075393.2,