rs63750938

Orientation

plus

Stabilized

plus

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

Make rs63750938(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017555

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750938
dbSNP (classic)	rs63750938
ClinGen	rs63750938
ebi	rs63750938
HLI	rs63750938
Exac	rs63750938
Gnomad	rs63750938
Varsome	rs63750938
LitVar	rs63750938
Map	rs63750938
PheGenI	rs63750938
Biobank	rs63750938
1000 genomes	rs63750938
hgdp	rs63750938
ensembl	rs63750938
geneview	rs63750938
scholar	rs63750938
google	rs63750938
pharmgkb	rs63750938
gwascentral	rs63750938
openSNP	rs63750938
23andMe	rs63750938
SNPshot	rs63750938
SNPdbe	rs63750938
MSV3d	rs63750938
GWAS Ctlg	rs63750938

Max Magnitude

6

ClinVar
Risk	rs63750938(A;A) rs63750938(C;C)
Alt	rs63750938(A;A) rs63750938(C;C)
Reference	Rs63750938(T;T)
Significance	Pathogenic
Disease	Lynch syndrome not specified
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.37059046T>A; NC_000003.11:g.37059046T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075882.2, RCV000428497.1,