rs587778957

Orientation

plus

Stabilized

plus

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

Make rs587778957(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37048524

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778957
dbSNP (classic)	rs587778957
ClinGen	rs587778957
ebi	rs587778957
HLI	rs587778957
Exac	rs587778957
Gnomad	rs587778957
Varsome	rs587778957
LitVar	rs587778957
Map	rs587778957
PheGenI	rs587778957
Biobank	rs587778957
1000 genomes	rs587778957
hgdp	rs587778957
ensembl	rs587778957
geneview	rs587778957
scholar	rs587778957
google	rs587778957
pharmgkb	rs587778957
gwascentral	rs587778957
openSNP	rs587778957
23andMe	rs587778957
SNPshot	rs587778957
SNPdbe	rs587778957
MSV3d	rs587778957
GWAS Ctlg	rs587778957

Max Magnitude

6

ClinVar
Risk	rs587778957(A;A)
Alt	rs587778957(A;A)
Reference	Rs587778957(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090015dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075417.2,