rs1057516963

Orientation

minus

Stabilized

minus

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

Make rs1057516963(G;T)

Make rs1057516963(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95107101

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs1057516963
dbSNP (classic)	rs1057516963
ClinGen	rs1057516963
ebi	rs1057516963
HLI	rs1057516963
Exac	rs1057516963
Gnomad	rs1057516963
Varsome	rs1057516963
LitVar	rs1057516963
Map	rs1057516963
PheGenI	rs1057516963
Biobank	rs1057516963
1000 genomes	rs1057516963
hgdp	rs1057516963
ensembl	rs1057516963
geneview	rs1057516963
scholar	rs1057516963
google	rs1057516963
pharmgkb	rs1057516963
gwascentral	rs1057516963
openSNP	rs1057516963
23andMe	rs1057516963
SNPshot	rs1057516963
SNPdbe	rs1057516963
MSV3d	rs1057516963
GWAS Ctlg	rs1057516963

Max Magnitude

0

ClinVar
Risk	rs1057516963(T;T)
Alt	rs1057516963(T;T)
Reference	Rs1057516963(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97869383C>A
CLNSRC
CLNACC	RCV000409084.1,