Original source

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

Alleles
TA/- | MAF: 0.16 (-)
Location

Chromosome 1:113849585-113849586 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147702491

This variation has 9 HGVS names - click the plus to show

Variation displays