rs1057517170

Orientation

minus

Stabilized

minus

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

Make rs1057517170(C;C)

Make rs1057517170(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95107064

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs1057517170
dbSNP (classic)	rs1057517170
ClinGen	rs1057517170
ebi	rs1057517170
HLI	rs1057517170
Exac	rs1057517170
Gnomad	rs1057517170
Varsome	rs1057517170
LitVar	rs1057517170
Map	rs1057517170
PheGenI	rs1057517170
Biobank	rs1057517170
1000 genomes	rs1057517170
hgdp	rs1057517170
ensembl	rs1057517170
geneview	rs1057517170
scholar	rs1057517170
google	rs1057517170
pharmgkb	rs1057517170
gwascentral	rs1057517170
openSNP	rs1057517170
23andMe	rs1057517170
SNPshot	rs1057517170
SNPdbe	rs1057517170
MSV3d	rs1057517170
GWAS Ctlg	rs1057517170

Max Magnitude

0

ClinVar
Risk	rs1057517170(C;C)
Alt	rs1057517170(C;C)
Reference	Rs1057517170(T;T)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97869346A>G
CLNSRC
CLNACC	RCV000410650.1,