rs121912958

Merged into

rs63751615

Orientation

plus

Stabilized

plus

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

Make rs121912958(C;T)

Make rs121912958(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37012098

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs121912958
dbSNP (classic)	rs121912958
ClinGen	rs121912958
ebi	rs121912958
HLI	rs121912958
Exac	rs121912958
Gnomad	rs121912958
Varsome	rs121912958
LitVar	rs121912958
Map	rs121912958
PheGenI	rs121912958
Biobank	rs121912958
1000 genomes	rs121912958
hgdp	rs121912958
ensembl	rs121912958
geneview	rs121912958
scholar	rs121912958
google	rs121912958
pharmgkb	rs121912958
gwascentral	rs121912958
openSNP	rs121912958
23andMe	rs121912958
SNPshot	rs121912958
SNPdbe	rs121912958
MSV3d	rs121912958
GWAS Ctlg	rs121912958

Status

Merged into rs63751615

Max Magnitude

0

OMIM	120436
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121912958(T;T)
Alt	rs121912958(T;T)
Reference	Rs121912958(C;C)
Significance	Pathogenic
Disease	Lynch syndrome II Turcot syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome II Turcot syndrome
Reversed	0
HGVS	NC_000003.11:g.37053589C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000038899.1, SCV000038900.1,