rs786204885

Merged into

rs587781340

Orientation

plus

Stabilized

plus

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

Make rs786204885(-;-)

Make rs786204885(-;AAGCCGCAGCAA)

Make rs786204885(AAGCCGCAGCAA;AAGCCGCAGCAA)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87863274

Gene	KLLN, PTEN

is a	snp
is	mentioned by
dbSNP	rs786204885
dbSNP (classic)	rs786204885
ClinGen	rs786204885
ebi	rs786204885
HLI	rs786204885
Exac	rs786204885
Gnomad	rs786204885
Varsome	rs786204885
LitVar	rs786204885
Map	rs786204885
PheGenI	rs786204885
Biobank	rs786204885
1000 genomes	rs786204885
hgdp	rs786204885
ensembl	rs786204885
geneview	rs786204885
scholar	rs786204885
google	rs786204885
pharmgkb	rs786204885
gwascentral	rs786204885
openSNP	rs786204885
23andMe	rs786204885
SNPshot	rs786204885
SNPdbe	rs786204885
MSV3d	rs786204885
GWAS Ctlg	rs786204885

Status

Merged into rs587781340

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786204885(GCAAAAGCCGCA;GCAAAAGCCGCA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	PTEN LOC101929706 KLLN
CLNDBN	Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000010.10:g.89623031_89623042delAAGCCGCAGCAA
CLNSRC	GeneDx
CLNACC	RCV000129113.4, RCV000169826.2,