rs774209201

Orientation

plus

Stabilized

plus

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

Make rs774209201(C;G)

Make rs774209201(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95126582

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs774209201
dbSNP (classic)	rs774209201
ClinGen	rs774209201
ebi	rs774209201
HLI	rs774209201
Exac	rs774209201
Gnomad	rs774209201
Varsome	rs774209201
LitVar	rs774209201
Map	rs774209201
PheGenI	rs774209201
Biobank	rs774209201
1000 genomes	rs774209201
hgdp	rs774209201
ensembl	rs774209201
geneview	rs774209201
scholar	rs774209201
google	rs774209201
pharmgkb	rs774209201
gwascentral	rs774209201
openSNP	rs774209201
23andMe	rs774209201
SNPshot	rs774209201
SNPdbe	rs774209201
MSV3d	rs774209201
GWAS Ctlg	rs774209201

Max Magnitude

0

ClinVar
Risk	rs774209201(G;G)
Alt	rs774209201(G;G)
Reference	Rs774209201(C;C)
Significance	Pathogenic
Disease	Fanconi anemia not provided Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C not provided Fanconi anemia
Reversed	0
HGVS	NC_000009.11:g.97888864C>G
CLNSRC
CLNACC	RCV000169449.1, RCV000224795.2, RCV000462508.1,