Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 3:47657937 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7372942

This variation has 3 HGVS names - click the plus to show

3:g.47657937C>T
ENST00000425518.3:n.2210+3357G>A
ENST00000254480.7:c.2320+3357G>A

Variation displays