rs121908984

Orientation

plus

Stabilized

plus

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

Make rs121908984(A;A)

Make rs121908984(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112094923

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs121908984
dbSNP (classic)	rs121908984
ClinGen	rs121908984
ebi	rs121908984
HLI	rs121908984
Exac	rs121908984
Gnomad	rs121908984
Varsome	rs121908984
LitVar	rs121908984
Map	rs121908984
PheGenI	rs121908984
Biobank	rs121908984
1000 genomes	rs121908984
hgdp	rs121908984
ensembl	rs121908984
geneview	rs121908984
scholar	rs121908984
google	rs121908984
pharmgkb	rs121908984
gwascentral	rs121908984
openSNP	rs121908984
23andMe	rs121908984
SNPshot	rs121908984
SNPdbe	rs121908984
MSV3d	rs121908984
GWAS Ctlg	rs121908984

Max Magnitude

0

OMIM	602690
Desc
Variant	0028
Related	also

ClinVar
Risk	rs121908984(A;A)
Alt	rs121908984(A;A)
Reference	Rs121908984(C;C)
Significance	Pathogenic
Disease	Cowden syndrome 3
Variation	info
Gene	SDHD
CLNDBN	Cowden syndrome 3
Reversed	0
HGVS	NC_000011.9:g.111965647C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007327.4,