rs1057516792

Orientation

minus

Stabilized

minus

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

Make rs1057516792(-;-)

Make rs1057516792(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95135358

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516792
dbSNP (classic)	rs1057516792
ClinGen	rs1057516792
ebi	rs1057516792
HLI	rs1057516792
Exac	rs1057516792
Gnomad	rs1057516792
Varsome	rs1057516792
LitVar	rs1057516792
Map	rs1057516792
PheGenI	rs1057516792
Biobank	rs1057516792
1000 genomes	rs1057516792
hgdp	rs1057516792
ensembl	rs1057516792
geneview	rs1057516792
scholar	rs1057516792
google	rs1057516792
pharmgkb	rs1057516792
gwascentral	rs1057516792
openSNP	rs1057516792
23andMe	rs1057516792
SNPshot	rs1057516792
SNPdbe	rs1057516792
MSV3d	rs1057516792
GWAS Ctlg	rs1057516792

Max Magnitude

0

ClinVar
Risk	rs1057516792(-;-)
Alt	rs1057516792(-;-)
Reference	Rs1057516792(A;A)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97897640delT
CLNSRC
CLNACC	RCV000410893.1,