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SNP
ks620569707

Organism
Homo sapiens
Study
kstd16
RS ID
rs1184001364
Submitted date
2026-05-13
Molecular Type
Genomic
Publication
Unpublished
Method Type
Sequencing
Variant Type
SNV
Sample Size
1
Position
chr16:62713981
Population
Korean
Alleles
T > C
Frequency
0.00757576

Genomic regions, transcriptions, and products
Cytoband
Scale
Ref.hg38
RefSeqGene
GENCODE
KVAR

Genomic Placement
Sequence name Change
GRCh38
chr16
chr16.
62713981
T > C