rs1060501878

Orientation

minus

Stabilized

minus

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

Make rs1060501878(A;T)

Make rs1060501878(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

89773304

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs1060501878
dbSNP (classic)	rs1060501878
ClinGen	rs1060501878
ebi	rs1060501878
HLI	rs1060501878
Exac	rs1060501878
Gnomad	rs1060501878
Varsome	rs1060501878
LitVar	rs1060501878
Map	rs1060501878
PheGenI	rs1060501878
Biobank	rs1060501878
1000 genomes	rs1060501878
hgdp	rs1060501878
ensembl	rs1060501878
geneview	rs1060501878
scholar	rs1060501878
google	rs1060501878
pharmgkb	rs1060501878
gwascentral	rs1060501878
openSNP	rs1060501878
23andMe	rs1060501878
SNPshot	rs1060501878
SNPdbe	rs1060501878
MSV3d	rs1060501878
GWAS Ctlg	rs1060501878

Max Magnitude

0

ClinVar
Risk	rs1060501878(T;T)
Alt	rs1060501878(T;T)
Reference	Rs1060501878(A;A)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCA
CLNDBN	Fanconi anemia
Reversed	1
HGVS	NC_000016.9:g.89839712T>A
CLNSRC
CLNACC	RCV000475930.1,