rs587778938

Orientation

plus

Stabilized

plus

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

Make rs587778938(ATTT;ATTT)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37040296

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778938
dbSNP (classic)	rs587778938
ClinGen	rs587778938
ebi	rs587778938
HLI	rs587778938
Exac	rs587778938
Gnomad	rs587778938
Varsome	rs587778938
LitVar	rs587778938
Map	rs587778938
PheGenI	rs587778938
Biobank	rs587778938
1000 genomes	rs587778938
hgdp	rs587778938
ensembl	rs587778938
geneview	rs587778938
scholar	rs587778938
google	rs587778938
pharmgkb	rs587778938
gwascentral	rs587778938
openSNP	rs587778938
23andMe	rs587778938
SNPshot	rs587778938
SNPdbe	rs587778938
MSV3d	rs587778938
GWAS Ctlg	rs587778938

Max Magnitude

6

ClinVar
Risk	rs587778938(ATTT;ATTT)
Alt	rs587778938(ATTT;ATTT)
Reference	Rs587778938(TAAATCA;TAAATCA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37081787_37081793delTAAATCAinsATTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075298.2,