rs1057516455

Orientation

minus

Stabilized

minus

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

Make rs1057516455(A;A)

Make rs1057516455(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95101785

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516455
dbSNP (classic)	rs1057516455
ClinGen	rs1057516455
ebi	rs1057516455
HLI	rs1057516455
Exac	rs1057516455
Gnomad	rs1057516455
Varsome	rs1057516455
LitVar	rs1057516455
Map	rs1057516455
PheGenI	rs1057516455
Biobank	rs1057516455
1000 genomes	rs1057516455
hgdp	rs1057516455
ensembl	rs1057516455
geneview	rs1057516455
scholar	rs1057516455
google	rs1057516455
pharmgkb	rs1057516455
gwascentral	rs1057516455
openSNP	rs1057516455
23andMe	rs1057516455
SNPshot	rs1057516455
SNPdbe	rs1057516455
MSV3d	rs1057516455
GWAS Ctlg	rs1057516455

Max Magnitude

0

ClinVar
Risk	rs1057516455(A;A)
Alt	rs1057516455(A;A)
Reference	Rs1057516455(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97864067C>T
CLNSRC
CLNACC	RCV000411700.1,