rs63749916

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

3

Position

37028894

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749916
dbSNP (classic)	rs63749916
ClinGen	rs63749916
ebi	rs63749916
HLI	rs63749916
Exac	rs63749916
Gnomad	rs63749916
Varsome	rs63749916
LitVar	rs63749916
Map	rs63749916
PheGenI	rs63749916
Biobank	rs63749916
1000 genomes	rs63749916
hgdp	rs63749916
ensembl	rs63749916
geneview	rs63749916
scholar	rs63749916
google	rs63749916
pharmgkb	rs63749916
gwascentral	rs63749916
openSNP	rs63749916
23andMe	rs63749916
SNPshot	rs63749916
SNPdbe	rs63749916
MSV3d	rs63749916
GWAS Ctlg	rs63749916

Max Magnitude

6

ClinVar
Risk	Rs63749916(T;T) rs63749916(TA;TA)
Alt	Rs63749916(T;T) rs63749916(TA;TA)
Reference	Rs63749916(-;-)
Significance	Pathogenic
Disease	not provided Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	not provided Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37070385_37070386insTA; NC_000003.11:g.37070385dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000216066.1, RCV000075233.2,