rs63751421

Orientation

plus

Stabilized

plus

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

Make rs63751421(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001003

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751421
dbSNP (classic)	rs63751421
ClinGen	rs63751421
ebi	rs63751421
HLI	rs63751421
Exac	rs63751421
Gnomad	rs63751421
Varsome	rs63751421
LitVar	rs63751421
Map	rs63751421
PheGenI	rs63751421
Biobank	rs63751421
1000 genomes	rs63751421
hgdp	rs63751421
ensembl	rs63751421
geneview	rs63751421
scholar	rs63751421
google	rs63751421
pharmgkb	rs63751421
gwascentral	rs63751421
openSNP	rs63751421
23andMe	rs63751421
SNPshot	rs63751421
SNPdbe	rs63751421
MSV3d	rs63751421
GWAS Ctlg	rs63751421

Max Magnitude

6

ClinVar
Risk	rs63751421(T;T)
Alt	rs63751421(T;T)
Reference	Rs63751421(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37042494C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075607.2,