rs1057516298

Orientation

minus

Stabilized

minus

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

Make rs1057516298(C;T)

Make rs1057516298(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95107266

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs1057516298
dbSNP (classic)	rs1057516298
ClinGen	rs1057516298
ebi	rs1057516298
HLI	rs1057516298
Exac	rs1057516298
Gnomad	rs1057516298
Varsome	rs1057516298
LitVar	rs1057516298
Map	rs1057516298
PheGenI	rs1057516298
Biobank	rs1057516298
1000 genomes	rs1057516298
hgdp	rs1057516298
ensembl	rs1057516298
geneview	rs1057516298
scholar	rs1057516298
google	rs1057516298
pharmgkb	rs1057516298
gwascentral	rs1057516298
openSNP	rs1057516298
23andMe	rs1057516298
SNPshot	rs1057516298
SNPdbe	rs1057516298
MSV3d	rs1057516298
GWAS Ctlg	rs1057516298

Max Magnitude

0

ClinVar
Risk	rs1057516298(T;T)
Alt	rs1057516298(T;T)
Reference	Rs1057516298(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.97869548G>A
CLNSRC
CLNACC	RCV000409733.1,