rs587778887

Orientation

plus

Stabilized

plus

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

Make rs587778887(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025730

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778887
dbSNP (classic)	rs587778887
ClinGen	rs587778887
ebi	rs587778887
HLI	rs587778887
Exac	rs587778887
Gnomad	rs587778887
Varsome	rs587778887
LitVar	rs587778887
Map	rs587778887
PheGenI	rs587778887
Biobank	rs587778887
1000 genomes	rs587778887
hgdp	rs587778887
ensembl	rs587778887
geneview	rs587778887
scholar	rs587778887
google	rs587778887
pharmgkb	rs587778887
gwascentral	rs587778887
openSNP	rs587778887
23andMe	rs587778887
SNPshot	rs587778887
SNPdbe	rs587778887
MSV3d	rs587778887
GWAS Ctlg	rs587778887

Max Magnitude

6

ClinVar
Risk	rs587778887(A;A)
Alt	rs587778887(A;A)
Reference	Rs587778887(GTC;GTC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067221_37067223delGTCinsA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075117.2,