rs1057516248

Orientation

minus

Stabilized

minus

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

Make rs1057516248(-;C)

Make rs1057516248(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95117349

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516248
dbSNP (classic)	rs1057516248
ClinGen	rs1057516248
ebi	rs1057516248
HLI	rs1057516248
Exac	rs1057516248
Gnomad	rs1057516248
Varsome	rs1057516248
LitVar	rs1057516248
Map	rs1057516248
PheGenI	rs1057516248
Biobank	rs1057516248
1000 genomes	rs1057516248
hgdp	rs1057516248
ensembl	rs1057516248
geneview	rs1057516248
scholar	rs1057516248
google	rs1057516248
pharmgkb	rs1057516248
gwascentral	rs1057516248
openSNP	rs1057516248
23andMe	rs1057516248
SNPshot	rs1057516248
SNPdbe	rs1057516248
MSV3d	rs1057516248
GWAS Ctlg	rs1057516248

Max Magnitude

0

ClinVar
Risk	rs1057516248(C;C)
Alt	rs1057516248(C;C)
Reference	Rs1057516248(-;-)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97879632dupG
CLNSRC
CLNACC	RCV000409572.1,