rs121913122

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	5	Hereditary leiomyomatosis and renal cell cancer

Make rs121913122(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

241504123

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs121913122
dbSNP (classic)	rs121913122
ClinGen	rs121913122
ebi	rs121913122
HLI	rs121913122
Exac	rs121913122
Gnomad	rs121913122
Varsome	rs121913122
LitVar	rs121913122
Map	rs121913122
PheGenI	rs121913122
Biobank	rs121913122
1000 genomes	rs121913122
hgdp	rs121913122
ensembl	rs121913122
geneview	rs121913122
scholar	rs121913122
google	rs121913122
pharmgkb	rs121913122
gwascentral	rs121913122
openSNP	rs121913122
23andMe	rs121913122
SNPshot	rs121913122
SNPdbe	rs121913122
MSV3d	rs121913122
GWAS Ctlg	rs121913122

Max Magnitude

5

OMIM	136850
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913122(T;T)
Alt	rs121913122(T;T)
Reference	Rs121913122(C;C)
Significance	Pathogenic
Disease	Hereditary leiomyomatosis and renal cell cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	FH
CLNDBN	Hereditary leiomyomatosis and renal cell cancer Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.241667423G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017622.24, RCV000130875.3, RCV000197989.2,