rs1057516488

Orientation

minus

Stabilized

minus

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

Make rs1057516488(A;A)

Make rs1057516488(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95107082

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs1057516488
dbSNP (classic)	rs1057516488
ClinGen	rs1057516488
ebi	rs1057516488
HLI	rs1057516488
Exac	rs1057516488
Gnomad	rs1057516488
Varsome	rs1057516488
LitVar	rs1057516488
Map	rs1057516488
PheGenI	rs1057516488
Biobank	rs1057516488
1000 genomes	rs1057516488
hgdp	rs1057516488
ensembl	rs1057516488
geneview	rs1057516488
scholar	rs1057516488
google	rs1057516488
pharmgkb	rs1057516488
gwascentral	rs1057516488
openSNP	rs1057516488
23andMe	rs1057516488
SNPshot	rs1057516488
SNPdbe	rs1057516488
MSV3d	rs1057516488
GWAS Ctlg	rs1057516488

Max Magnitude

0

ClinVar
Risk	rs1057516488(A;A)
Alt	rs1057516488(A;A)
Reference	Rs1057516488(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.97869364C>T
CLNSRC
CLNACC	RCV000409398.1,