rs863224965

Orientation

plus

Stabilized

plus

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

Make rs863224965(-;-)

Make rs863224965(-;TCCTACGAAGCTCTGAAAGGT)

Make rs863224965(TCCTACGAAGCTCTGAAAGGT;TCCTACGAAGCTCTGAAAGGT)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

42388938

Gene

CAPN3

is a	snp
is	mentioned by
dbSNP	rs863224965
dbSNP (classic)	rs863224965
ClinGen	rs863224965
ebi	rs863224965
HLI	rs863224965
Exac	rs863224965
Gnomad	rs863224965
Varsome	rs863224965
LitVar	rs863224965
Map	rs863224965
PheGenI	rs863224965
Biobank	rs863224965
1000 genomes	rs863224965
hgdp	rs863224965
ensembl	rs863224965
geneview	rs863224965
scholar	rs863224965
google	rs863224965
pharmgkb	rs863224965
gwascentral	rs863224965
openSNP	rs863224965
23andMe	rs863224965
SNPshot	rs863224965
SNPdbe	rs863224965
MSV3d	rs863224965
GWAS Ctlg	rs863224965

Max Magnitude

0

ClinVar
Risk	rs863224965(-;-) Rs863224965(GGTTCCTACGAAGCTCTGAAA;GGTTCCTACGAAGCTCTGAAA)
Alt	rs863224965(-;-) Rs863224965(GGTTCCTACGAAGCTCTGAAA;GGTTCCTACGAAGCTCTGAAA)
Reference	rs863224965(TCCTACGAAGCTCTGAAAGGT;TCCTACGAAGCTCTGAAAGGT)
Significance	Other
Disease	Limb-girdle muscular dystrophy not provided
Variation	info
Gene	CAPN3
CLNDBN	Limb-girdle muscular dystrophy, type 2A not provided
Reversed	0
HGVS	NC_000015.9:g.42681136_42681156del21
CLNSRC	Quest Diagnostics
CLNACC	RCV000201156.2, RCV000379696.1,