rs1057516420

Orientation

minus

Stabilized

minus

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

Make rs1057516420(C;T)

Make rs1057516420(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95111483

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516420
dbSNP (classic)	rs1057516420
ClinGen	rs1057516420
ebi	rs1057516420
HLI	rs1057516420
Exac	rs1057516420
Gnomad	rs1057516420
Varsome	rs1057516420
LitVar	rs1057516420
Map	rs1057516420
PheGenI	rs1057516420
Biobank	rs1057516420
1000 genomes	rs1057516420
hgdp	rs1057516420
ensembl	rs1057516420
geneview	rs1057516420
scholar	rs1057516420
google	rs1057516420
pharmgkb	rs1057516420
gwascentral	rs1057516420
openSNP	rs1057516420
23andMe	rs1057516420
SNPshot	rs1057516420
SNPdbe	rs1057516420
MSV3d	rs1057516420
GWAS Ctlg	rs1057516420

Max Magnitude

0

ClinVar
Risk	rs1057516420(T;T)
Alt	rs1057516420(T;T)
Reference	Rs1057516420(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.97873765G>A
CLNSRC
CLNACC	RCV000411906.1,