rs1060502605

Orientation

plus

Stabilized

plus

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

Make rs1060502605(-;-)

Make rs1060502605(-;ATCA)

Make rs1060502605(ATCA;ATCA)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

58720759

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs1060502605
dbSNP (classic)	rs1060502605
ClinGen	rs1060502605
ebi	rs1060502605
HLI	rs1060502605
Exac	rs1060502605
Gnomad	rs1060502605
Varsome	rs1060502605
LitVar	rs1060502605
Map	rs1060502605
PheGenI	rs1060502605
Biobank	rs1060502605
1000 genomes	rs1060502605
hgdp	rs1060502605
ensembl	rs1060502605
geneview	rs1060502605
scholar	rs1060502605
google	rs1060502605
pharmgkb	rs1060502605
gwascentral	rs1060502605
openSNP	rs1060502605
23andMe	rs1060502605
SNPshot	rs1060502605
SNPdbe	rs1060502605
MSV3d	rs1060502605
GWAS Ctlg	rs1060502605

Max Magnitude

0

ClinVar
Risk	rs1060502605(-;-)
Alt	rs1060502605(-;-)
Reference	Rs1060502605(CAAT;CAAT)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56798120_56798123delATCA
CLNSRC
CLNACC	RCV000465331.1,