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rs761991070

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs761991070(A;G)
Make rs761991070(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position88655350
GeneMVD
is asnp
is mentioned by
dbSNPrs761991070
ebirs761991070
HLIrs761991070
Exacrs761991070
Varsomers761991070
Maprs761991070
PheGenIrs761991070
hapmaprs761991070
1000 genomesrs761991070
hgdprs761991070
ensemblrs761991070
gopubmedrs761991070
geneviewrs761991070
scholarrs761991070
googlers761991070
pharmgkbrs761991070
gwascentralrs761991070
openSNPrs761991070
23andMers761991070
23andMe allrs761991070
SNP Nexus

SNPshotrs761991070
SNPdbers761991070
MSV3drs761991070
GWAS Ctlgrs761991070
Max Magnitude0
ClinVar
Risk rs761991070(G;G)
Alt rs761991070(G;G)
Reference rs761991070(A;A)
Significance Pathogenic
Disease Porokeratosis 7
Variation info
Gene MVD
CLNDBN Porokeratosis 7, multiple types
Reversed 0
HGVS NC_000016.9:g.88721758A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000239486.1,