rs1060502601

Orientation

plus

Stabilized

plus

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

Make rs1060502601(-;-)

Make rs1060502601(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

58709885

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs1060502601
dbSNP (classic)	rs1060502601
ClinGen	rs1060502601
ebi	rs1060502601
HLI	rs1060502601
Exac	rs1060502601
Gnomad	rs1060502601
Varsome	rs1060502601
LitVar	rs1060502601
Map	rs1060502601
PheGenI	rs1060502601
Biobank	rs1060502601
1000 genomes	rs1060502601
hgdp	rs1060502601
ensembl	rs1060502601
geneview	rs1060502601
scholar	rs1060502601
google	rs1060502601
pharmgkb	rs1060502601
gwascentral	rs1060502601
openSNP	rs1060502601
23andMe	rs1060502601
SNPshot	rs1060502601
SNPdbe	rs1060502601
MSV3d	rs1060502601
GWAS Ctlg	rs1060502601

Max Magnitude

0

ClinVar
Risk	rs1060502601(-;-)
Alt	rs1060502601(-;-)
Reference	Rs1060502601(T;T)
Significance	Pathogenic
Disease	Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56787246delT
CLNSRC
CLNACC	RCV000471345.1, RCV000486595.1,