rs121918338

Orientation

minus

Stabilized

minus

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

Make rs121918338(C;T)

Make rs121918338(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

136370362

Gene

CARD9

is a	snp
is	mentioned by
dbSNP	rs121918338
dbSNP (classic)	rs121918338
ClinGen	rs121918338
ebi	rs121918338
HLI	rs121918338
Exac	rs121918338
Gnomad	rs121918338
Varsome	rs121918338
LitVar	rs121918338
Map	rs121918338
PheGenI	rs121918338
Biobank	rs121918338
1000 genomes	rs121918338
hgdp	rs121918338
ensembl	rs121918338
geneview	rs121918338
scholar	rs121918338
google	rs121918338
pharmgkb	rs121918338
gwascentral	rs121918338
openSNP	rs121918338
23andMe	rs121918338
SNPshot	rs121918338
SNPdbe	rs121918338
MSV3d	rs121918338
GWAS Ctlg	rs121918338

Max Magnitude

0

OMIM	607212
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918338(T;T)
Alt	rs121918338(T;T)
Reference	Rs121918338(C;C)
Significance	Pathogenic
Disease	Candidiasis
Variation	info
Gene	CARD9 DNLZ
CLNDBN	Candidiasis, familial, 2
Reversed	1
HGVS	NC_000009.11:g.139264814G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003575.2,