rs1057521855

Orientation

minus

Stabilized

minus

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

Make rs1057521855(C;T)

Make rs1057521855(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

89783084

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs1057521855
dbSNP (classic)	rs1057521855
ClinGen	rs1057521855
ebi	rs1057521855
HLI	rs1057521855
Exac	rs1057521855
Gnomad	rs1057521855
Varsome	rs1057521855
LitVar	rs1057521855
Map	rs1057521855
PheGenI	rs1057521855
Biobank	rs1057521855
1000 genomes	rs1057521855
hgdp	rs1057521855
ensembl	rs1057521855
geneview	rs1057521855
scholar	rs1057521855
google	rs1057521855
pharmgkb	rs1057521855
gwascentral	rs1057521855
openSNP	rs1057521855
23andMe	rs1057521855
SNPshot	rs1057521855
SNPdbe	rs1057521855
MSV3d	rs1057521855
GWAS Ctlg	rs1057521855

Max Magnitude

0

ClinVar
Risk	rs1057521855(T;T)
Alt	rs1057521855(T;T)
Reference	Rs1057521855(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCA
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.89849492G>A
CLNSRC
CLNACC	RCV000432541.1,