rs121912959

Merged into

rs63750206

Orientation

plus

Stabilized

plus

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

Make rs121912959(G;T)

Make rs121912959(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996701

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs121912959
dbSNP (classic)	rs121912959
ClinGen	rs121912959
ebi	rs121912959
HLI	rs121912959
Exac	rs121912959
Gnomad	rs121912959
Varsome	rs121912959
LitVar	rs121912959
Map	rs121912959
PheGenI	rs121912959
Biobank	rs121912959
1000 genomes	rs121912959
hgdp	rs121912959
ensembl	rs121912959
geneview	rs121912959
scholar	rs121912959
google	rs121912959
pharmgkb	rs121912959
gwascentral	rs121912959
openSNP	rs121912959
23andMe	rs121912959
SNPshot	rs121912959
SNPdbe	rs121912959
MSV3d	rs121912959
GWAS Ctlg	rs121912959

Status

Merged into rs63750206

Max Magnitude

0

OMIM	120436
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121912959(T;T)
Alt	rs121912959(T;T)
Reference	Rs121912959(G;G)
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.37038192G>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000038901.1, SCV000038902.1,