rs878853780

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs878853780(C;C)

Make rs878853780(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

37040296

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs878853780
dbSNP (classic)	rs878853780
ClinGen	rs878853780
ebi	rs878853780
HLI	rs878853780
Exac	rs878853780
Gnomad	rs878853780
Varsome	rs878853780
LitVar	rs878853780
Map	rs878853780
PheGenI	rs878853780
Biobank	rs878853780
1000 genomes	rs878853780
hgdp	rs878853780
ensembl	rs878853780
geneview	rs878853780
scholar	rs878853780
google	rs878853780
pharmgkb	rs878853780
gwascentral	rs878853780
openSNP	rs878853780
23andMe	rs878853780
SNPshot	rs878853780
SNPdbe	rs878853780
MSV3d	rs878853780
GWAS Ctlg	rs878853780

Max Magnitude

0

ClinVar
Risk	rs878853780(C;C)
Alt	rs878853780(C;C)
Reference	Rs878853780(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37081787T>C
CLNSRC
CLNACC	RCV000231513.1,