rs756367276

Orientation

plus

Stabilized

plus

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

Make rs756367276(-;A)

Make rs756367276(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

89761961

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs756367276
dbSNP (classic)	rs756367276
ClinGen	rs756367276
ebi	rs756367276
HLI	rs756367276
Exac	rs756367276
Gnomad	rs756367276
Varsome	rs756367276
LitVar	rs756367276
Map	rs756367276
PheGenI	rs756367276
Biobank	rs756367276
1000 genomes	rs756367276
hgdp	rs756367276
ensembl	rs756367276
geneview	rs756367276
scholar	rs756367276
google	rs756367276
pharmgkb	rs756367276
gwascentral	rs756367276
openSNP	rs756367276
23andMe	rs756367276
SNPshot	rs756367276
SNPdbe	rs756367276
MSV3d	rs756367276
GWAS Ctlg	rs756367276

Max Magnitude

0

ClinVar
Risk	rs756367276(A;A)
Alt	rs756367276(A;A)
Reference	Rs756367276(-;-)
Significance	Pathogenic
Disease	Fanconi anemia Fanconi anemia
Variation	info
Gene	FANCA
CLNDBN	Fanconi anemia Fanconi anemia, complementation group A
Reversed	0
HGVS	NC_000016.9:g.89828370dupA
CLNSRC
CLNACC	RCV000168438.2, RCV000239378.1,