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
ENST00000341360.5:c.193+1498G>T
ENST00000367218.6:c.193+1498G>T
ENST00000357681.8:c.193+1498G>T

About this variant

This variant overlaps 3 transcripts, has 1112 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays