rs1057517125

Orientation

minus

Stabilized

minus

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

Make rs1057517125(G;T)

Make rs1057517125(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95149922

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057517125
dbSNP (classic)	rs1057517125
ClinGen	rs1057517125
ebi	rs1057517125
HLI	rs1057517125
Exac	rs1057517125
Gnomad	rs1057517125
Varsome	rs1057517125
LitVar	rs1057517125
Map	rs1057517125
PheGenI	rs1057517125
Biobank	rs1057517125
1000 genomes	rs1057517125
hgdp	rs1057517125
ensembl	rs1057517125
geneview	rs1057517125
scholar	rs1057517125
google	rs1057517125
pharmgkb	rs1057517125
gwascentral	rs1057517125
openSNP	rs1057517125
23andMe	rs1057517125
SNPshot	rs1057517125
SNPdbe	rs1057517125
MSV3d	rs1057517125
GWAS Ctlg	rs1057517125

Max Magnitude

0

ClinVar
Risk	rs1057517125(T;T)
Alt	rs1057517125(T;T)
Reference	Rs1057517125(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.97912204C>A
CLNSRC
CLNACC	RCV000409465.1,