Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V | MAF: < 0.01 (G)
Location

Chromosome 15:43203237 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NG_011505.1:g.22889G>T_1341605555

This variation has 24 HGVS names - click the plus to show

Variation displays