rs121912961

Merged into

rs63750781

Orientation

plus

Stabilized

plus

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

Make rs121912961(C;T)

Make rs121912961(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004444

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs121912961
dbSNP (classic)	rs121912961
ClinGen	rs121912961
ebi	rs121912961
HLI	rs121912961
Exac	rs121912961
Gnomad	rs121912961
Varsome	rs121912961
LitVar	rs121912961
Map	rs121912961
PheGenI	rs121912961
Biobank	rs121912961
1000 genomes	rs121912961
hgdp	rs121912961
ensembl	rs121912961
geneview	rs121912961
scholar	rs121912961
google	rs121912961
pharmgkb	rs121912961
gwascentral	rs121912961
openSNP	rs121912961
23andMe	rs121912961
SNPshot	rs121912961
SNPdbe	rs121912961
MSV3d	rs121912961
GWAS Ctlg	rs121912961

Status

Merged into rs63750781

Max Magnitude

0

OMIM	120436
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121912961(T;T)
Alt	rs121912961(T;T)
Reference	Rs121912961(C;C)
Significance	Pathogenic
Disease	Lynch syndrome II
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome II
Reversed	0
HGVS	NC_000003.11:g.37045935C>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000038909.1,