Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
ATTCCAG/- | MAF: < 0.01 (ATTCCAG)
Location

Chromosome 16:30747150-30747156 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs149647812

This variation has 2 HGVS names - click the plus to show

Variation displays