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rs672601338

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601338(C;C)
Make rs672601338(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position1270781
GeneBHLHA9
is asnp
is mentioned by
dbSNPrs672601338
ebirs672601338
HLIrs672601338
Exacrs672601338
Varsomers672601338
Maprs672601338
PheGenIrs672601338
hapmaprs672601338
1000 genomesrs672601338
hgdprs672601338
ensemblrs672601338
gopubmedrs672601338
geneviewrs672601338
scholarrs672601338
googlers672601338
pharmgkbrs672601338
gwascentralrs672601338
openSNPrs672601338
23andMers672601338
23andMe allrs672601338
SNP Nexus

SNPshotrs672601338
SNPdbers672601338
MSV3drs672601338
GWAS Ctlgrs672601338
Max Magnitude0
ClinVar
Risk rs672601338(C;C)
Alt rs672601338(C;C)
Reference rs672601338(G;G)
Significance Pathogenic
Disease Syndactyly type 9
Variation info
Gene BHLHA9
CLNDBN Syndactyly type 9
Reversed 0
HGVS NC_000017.10:g.1174075G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149487.5,