Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.15 (G)
Location

Chromosome 1:203684896 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60332666

This variation has 4 HGVS names - click the plus to show

1:g.203684896G>T
ENST00000341360.3:c.193+1498G>T
ENST00000367218.4:c.193+1498G>T
ENST00000357681.6:c.193+1498G>T

Variation displays