rs587778958

Orientation

plus

Stabilized

plus

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

Make rs587778958(GATTACCCCTTCTG;GATTACCCCTTCTG)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37048546

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778958
dbSNP (classic)	rs587778958
ClinGen	rs587778958
ebi	rs587778958
HLI	rs587778958
Exac	rs587778958
Gnomad	rs587778958
Varsome	rs587778958
LitVar	rs587778958
Map	rs587778958
PheGenI	rs587778958
Biobank	rs587778958
1000 genomes	rs587778958
hgdp	rs587778958
ensembl	rs587778958
geneview	rs587778958
scholar	rs587778958
google	rs587778958
pharmgkb	rs587778958
gwascentral	rs587778958
openSNP	rs587778958
23andMe	rs587778958
SNPshot	rs587778958
SNPdbe	rs587778958
MSV3d	rs587778958
GWAS Ctlg	rs587778958

Max Magnitude

6

ClinVar
Risk	rs587778958(TGGATTACCCCTTC;TGGATTACCCCTTC)
Alt	rs587778958(TGGATTACCCCTTC;TGGATTACCCCTTC)
Reference	Rs587778958(-;-)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37090024_37090037dupGATTACCCCTTCTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075421.2, RCV000202103.1,