rs867319477

Orientation

plus

Stabilized

plus

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

Make rs867319477(G;T)

Make rs867319477(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95101756

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs867319477
dbSNP (classic)	rs867319477
ClinGen	rs867319477
ebi	rs867319477
HLI	rs867319477
Exac	rs867319477
Gnomad	rs867319477
Varsome	rs867319477
LitVar	rs867319477
Map	rs867319477
PheGenI	rs867319477
Biobank	rs867319477
1000 genomes	rs867319477
hgdp	rs867319477
ensembl	rs867319477
geneview	rs867319477
scholar	rs867319477
google	rs867319477
pharmgkb	rs867319477
gwascentral	rs867319477
openSNP	rs867319477
23andMe	rs867319477
SNPshot	rs867319477
SNPdbe	rs867319477
MSV3d	rs867319477
GWAS Ctlg	rs867319477

Max Magnitude

0

ClinVar
Risk	rs867319477(T;T)
Alt	rs867319477(T;T)
Reference	Rs867319477(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	0
HGVS	NC_000009.11:g.97864038G>T
CLNSRC
CLNACC	RCV000409524.1,