SNP - NCBI

Format

Choose Destination

Select item 346188901.

rs34618890 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:68662588 (GRCh38)
4:69528306 (GRCh37)
Canonical SPDI:: NC_000004.12:68662587:C:A,NC_000004.12:68662587:C:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.04806/686 (ALFA)
T=0.02891/485 (TOMMO)
T=0.0411/120 (KOREAN)
T=0.2963/64 (Qatari)
C=0.5/37 (SGDP_PRJ)
HGVS:: NC_000004.12:g.68662588C>A, NC_000004.12:g.68662588C>T, NC_000004.11:g.69528306C>A, NC_000004.11:g.69528306C>T, NG_052676.1:g.13189G>T, NG_052676.1:g.13189G>A, NT_167250.2:g.238943C>A, NT_167250.2:g.238943C>T, NT_167250.1:g.240893C>A, NT_167250.1:g.240893C>T

dbSNP