rs267606693

Orientation

minus

Stabilized

minus

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

Make rs267606693(A;A)

Make rs267606693(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

63487491

Gene

WDPCP

is a	snp
is	mentioned by
dbSNP	rs267606693
dbSNP (classic)	rs267606693
ClinGen	rs267606693
ebi	rs267606693
HLI	rs267606693
Exac	rs267606693
Gnomad	rs267606693
Varsome	rs267606693
LitVar	rs267606693
Map	rs267606693
PheGenI	rs267606693
Biobank	rs267606693
1000 genomes	rs267606693
hgdp	rs267606693
ensembl	rs267606693
geneview	rs267606693
scholar	rs267606693
google	rs267606693
pharmgkb	rs267606693
gwascentral	rs267606693
openSNP	rs267606693
23andMe	rs267606693
SNPshot	rs267606693
SNPdbe	rs267606693
MSV3d	rs267606693
GWAS Ctlg	rs267606693

Max Magnitude

0

ClinVar
Risk	rs267606693(A;A)
Alt	rs267606693(A;A)
Reference	Rs267606693(G;G)
Significance	Other
Disease	Meckel syndrome
Variation	info
Gene	WDPCP
CLNDBN	Meckel syndrome, type 6, modifier of
Reversed	1
HGVS	NC_000002.11:g.63714625C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000064.5,