rs387907026

Orientation

minus

Stabilized

minus

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

Make rs387907026(C;T)

Make rs387907026(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

967282

Gene

RSPO4

is a	snp
is	mentioned by
dbSNP	rs387907026
dbSNP (classic)	rs387907026
ClinGen	rs387907026
ebi	rs387907026
HLI	rs387907026
Exac	rs387907026
Gnomad	rs387907026
Varsome	rs387907026
LitVar	rs387907026
Map	rs387907026
PheGenI	rs387907026
Biobank	rs387907026
1000 genomes	rs387907026
hgdp	rs387907026
ensembl	rs387907026
geneview	rs387907026
scholar	rs387907026
google	rs387907026
pharmgkb	rs387907026
gwascentral	rs387907026
openSNP	rs387907026
23andMe	rs387907026
SNPshot	rs387907026
SNPdbe	rs387907026
MSV3d	rs387907026
GWAS Ctlg	rs387907026

Max Magnitude

0

ClinVar
Risk	rs387907026(T;T)
Alt	rs387907026(T;T)
Reference	Rs387907026(C;C)
Significance	Pathogenic
Disease	Anonychia
Variation	info
Gene	RSPO4
CLNDBN	Anonychia
Reversed	1
HGVS	NC_000020.10:g.947925G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023830.2,