rs267607893

Orientation

plus

Stabilized

plus

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

Make rs267607893(C;G)

Make rs267607893(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

37050632

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607893
dbSNP (classic)	rs267607893
ClinGen	rs267607893
ebi	rs267607893
HLI	rs267607893
Exac	rs267607893
Gnomad	rs267607893
Varsome	rs267607893
LitVar	rs267607893
Map	rs267607893
PheGenI	rs267607893
Biobank	rs267607893
1000 genomes	rs267607893
hgdp	rs267607893
ensembl	rs267607893
geneview	rs267607893
scholar	rs267607893
google	rs267607893
pharmgkb	rs267607893
gwascentral	rs267607893
openSNP	rs267607893
23andMe	rs267607893
SNPshot	rs267607893
SNPdbe	rs267607893
MSV3d	rs267607893
GWAS Ctlg	rs267607893

Max Magnitude

0

ClinVar
Risk	rs267607893(A;A) rs267607893(G;G) rs267607893(T;T)
Alt	rs267607893(A;A) rs267607893(G;G) rs267607893(T;T)
Reference	Rs267607893(C;C)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37092123C>A; NC_000003.11:g.37092123C>G
CLNSRC
CLNACC	RCV000075584.2, RCV000075585.2, RCV000482247.1,