rs1057516291

Orientation

minus

Stabilized

minus

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

Make rs1057516291(A;A)

Make rs1057516291(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95240655

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057516291
dbSNP (classic)	rs1057516291
ClinGen	rs1057516291
ebi	rs1057516291
HLI	rs1057516291
Exac	rs1057516291
Gnomad	rs1057516291
Varsome	rs1057516291
LitVar	rs1057516291
Map	rs1057516291
PheGenI	rs1057516291
Biobank	rs1057516291
1000 genomes	rs1057516291
hgdp	rs1057516291
ensembl	rs1057516291
geneview	rs1057516291
scholar	rs1057516291
google	rs1057516291
pharmgkb	rs1057516291
gwascentral	rs1057516291
openSNP	rs1057516291
23andMe	rs1057516291
SNPshot	rs1057516291
SNPdbe	rs1057516291
MSV3d	rs1057516291
GWAS Ctlg	rs1057516291

Max Magnitude

0

ClinVar
Risk	rs1057516291(A;A)
Alt	rs1057516291(A;A)
Reference	Rs1057516291(G;G)
Significance	Pathogenic
Disease	Fanconi anemia Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.98002937C>T
CLNSRC
CLNACC	RCV000412313.1, RCV000462409.1,