rs730881935

Orientation

minus

Stabilized

minus

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

Make rs730881935(-;-)

Make rs730881935(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

35107105

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs730881935
dbSNP (classic)	rs730881935
ClinGen	rs730881935
ebi	rs730881935
HLI	rs730881935
Exac	rs730881935
Gnomad	rs730881935
Varsome	rs730881935
LitVar	rs730881935
Map	rs730881935
PheGenI	rs730881935
Biobank	rs730881935
1000 genomes	rs730881935
hgdp	rs730881935
ensembl	rs730881935
geneview	rs730881935
scholar	rs730881935
google	rs730881935
pharmgkb	rs730881935
gwascentral	rs730881935
openSNP	rs730881935
23andMe	rs730881935
SNPshot	rs730881935
SNPdbe	rs730881935
MSV3d	rs730881935
GWAS Ctlg	rs730881935

Max Magnitude

0

ClinVar
Risk	rs730881935(-;-)
Alt	rs730881935(-;-)
Reference	Rs730881935(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	RAD51D RAD51L3-RFFL
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.33434124delT
CLNSRC
CLNACC	RCV000160929.2, RCV000412677.1,