rs1060501862

Orientation

minus

Stabilized

minus

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

Make rs1060501862(A;A)

Make rs1060501862(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

35076970

Gene

FANCG

is a	snp
is	mentioned by
dbSNP	rs1060501862
dbSNP (old)	rs1060501862
ClinGen	rs1060501862
ebi	rs1060501862
HLI	rs1060501862
Exac	rs1060501862
Gnomad	rs1060501862
Varsome	rs1060501862
Map	rs1060501862
PheGenI	rs1060501862
Biobank	rs1060501862
1000 genomes	rs1060501862
hgdp	rs1060501862
ensembl	rs1060501862
gopubmed	rs1060501862
geneview	rs1060501862
scholar	rs1060501862
google	rs1060501862
pharmgkb	rs1060501862
gwascentral	rs1060501862
openSNP	rs1060501862
23andMe	rs1060501862
23andMe all	rs1060501862
SNPshot	rs1060501862
SNPdbe	rs1060501862
MSV3d	rs1060501862
GWAS Ctlg	rs1060501862

Max Magnitude

0

ClinVar
Risk	rs1060501862(A;A)
Alt	rs1060501862(A;A)
Reference	Rs1060501862(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCG
CLNDBN	Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.35076967C>T
CLNSRC
CLNACC	RCV000461878.1,