Have questions? Visit https://www.reddit.com/r/SNPedia

rs199624315

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199624315(G;T)
Make rs199624315(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position66638300
GeneKCTD7
is asnp
is mentioned by
dbSNPrs199624315
ebirs199624315
HLIrs199624315
Exacrs199624315
Varsomers199624315
Maprs199624315
PheGenIrs199624315
hapmaprs199624315
1000 genomesrs199624315
hgdprs199624315
ensemblrs199624315
gopubmedrs199624315
geneviewrs199624315
scholarrs199624315
googlers199624315
pharmgkbrs199624315
gwascentralrs199624315
openSNPrs199624315
23andMers199624315
23andMe allrs199624315
SNP Nexus

SNPshotrs199624315
SNPdbers199624315
MSV3drs199624315
GWAS Ctlgrs199624315
Max Magnitude0
ClinVar
Risk rs199624315(A,T;A,T)
Alt rs199624315(A,T;A,T)
Reference rs199624315(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCTD7
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.66103287G>T
CLNSRC
CLNACC RCV000188028.1,