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

rs876661307

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661307(C;C)
Make rs876661307(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position100123231
GeneSASS6
is asnp
is mentioned by
dbSNPrs876661307
ebirs876661307
HLIrs876661307
Exacrs876661307
Varsomers876661307
Maprs876661307
PheGenIrs876661307
hapmaprs876661307
1000 genomesrs876661307
hgdprs876661307
ensemblrs876661307
gopubmedrs876661307
geneviewrs876661307
scholarrs876661307
googlers876661307
pharmgkbrs876661307
gwascentralrs876661307
openSNPrs876661307
23andMers876661307
23andMe allrs876661307
SNP Nexus

SNPshotrs876661307
SNPdbers876661307
MSV3drs876661307
GWAS Ctlgrs876661307
Max Magnitude0
ClinVar
Risk rs876661307(C;C)
Alt rs876661307(C;C)
Reference rs876661307(T;T)
Significance Pathogenic
Disease Primary autosomal recessive microcephaly 14
Variation info
Gene SASS6
CLNDBN Primary autosomal recessive microcephaly 14
Reversed 1
HGVS NC_000001.10:g.100588787A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000172831.3,