rs1057516384

Orientation

minus

Stabilized

minus

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

Make rs1057516384(C;T)

Make rs1057516384(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95240687

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516384
dbSNP (classic)	rs1057516384
ClinGen	rs1057516384
ebi	rs1057516384
HLI	rs1057516384
Exac	rs1057516384
Gnomad	rs1057516384
Varsome	rs1057516384
LitVar	rs1057516384
Map	rs1057516384
PheGenI	rs1057516384
Biobank	rs1057516384
1000 genomes	rs1057516384
hgdp	rs1057516384
ensembl	rs1057516384
geneview	rs1057516384
scholar	rs1057516384
google	rs1057516384
pharmgkb	rs1057516384
gwascentral	rs1057516384
openSNP	rs1057516384
23andMe	rs1057516384
SNPshot	rs1057516384
SNPdbe	rs1057516384
MSV3d	rs1057516384
GWAS Ctlg	rs1057516384

Max Magnitude

0

ClinVar
Risk	rs1057516384(T;T)
Alt	rs1057516384(T;T)
Reference	Rs1057516384(C;C)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.98002969G>A
CLNSRC
CLNACC	RCV000412276.1,