rs63751310

Orientation

plus

Stabilized

plus

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

Make rs63751310(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048595

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751310
dbSNP (classic)	rs63751310
ClinGen	rs63751310
ebi	rs63751310
HLI	rs63751310
Exac	rs63751310
Gnomad	rs63751310
Varsome	rs63751310
LitVar	rs63751310
Map	rs63751310
PheGenI	rs63751310
Biobank	rs63751310
1000 genomes	rs63751310
hgdp	rs63751310
ensembl	rs63751310
geneview	rs63751310
scholar	rs63751310
google	rs63751310
pharmgkb	rs63751310
gwascentral	rs63751310
openSNP	rs63751310
23andMe	rs63751310
SNPshot	rs63751310
SNPdbe	rs63751310
MSV3d	rs63751310
GWAS Ctlg	rs63751310

Max Magnitude

6

ClinVar
Risk	rs63751310(T;T)
Alt	rs63751310(T;T)
Reference	Rs63751310(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37090086C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075444.2, RCV000128869.3, RCV000202252.2,