rs1057516917

Orientation

minus

Stabilized

minus

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

Make rs1057516917(G;T)

Make rs1057516917(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95171144

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516917
dbSNP (classic)	rs1057516917
ClinGen	rs1057516917
ebi	rs1057516917
HLI	rs1057516917
Exac	rs1057516917
Gnomad	rs1057516917
Varsome	rs1057516917
LitVar	rs1057516917
Map	rs1057516917
PheGenI	rs1057516917
Biobank	rs1057516917
1000 genomes	rs1057516917
hgdp	rs1057516917
ensembl	rs1057516917
geneview	rs1057516917
scholar	rs1057516917
google	rs1057516917
pharmgkb	rs1057516917
gwascentral	rs1057516917
openSNP	rs1057516917
23andMe	rs1057516917
SNPshot	rs1057516917
SNPdbe	rs1057516917
MSV3d	rs1057516917
GWAS Ctlg	rs1057516917

Max Magnitude

0

ClinVar
Risk	rs1057516917(T;T)
Alt	rs1057516917(T;T)
Reference	Rs1057516917(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.97933426C>A
CLNSRC
CLNACC	RCV000410360.1,