rs767796996

Orientation

plus

Stabilized

plus

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

Make rs767796996(A;A)

Make rs767796996(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58695189

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs767796996
dbSNP (classic)	rs767796996
ClinGen	rs767796996
ebi	rs767796996
HLI	rs767796996
Exac	rs767796996
Gnomad	rs767796996
Varsome	rs767796996
LitVar	rs767796996
Map	rs767796996
PheGenI	rs767796996
Biobank	rs767796996
1000 genomes	rs767796996
hgdp	rs767796996
ensembl	rs767796996
geneview	rs767796996
scholar	rs767796996
google	rs767796996
pharmgkb	rs767796996
gwascentral	rs767796996
openSNP	rs767796996
23andMe	rs767796996
SNPshot	rs767796996
SNPdbe	rs767796996
MSV3d	rs767796996
GWAS Ctlg	rs767796996

Max Magnitude

0

ClinVar
Risk	rs767796996(A;A) rs767796996(C;C)
Alt	rs767796996(A;A) rs767796996(C;C)
Reference	Rs767796996(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56772550G>A; NC_000017.10:g.56772550G>C
CLNSRC
CLNACC	RCV000217463.1, RCV000458645.1, RCV000478459.1,