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 | MAF: < 0.01 (T)
Location

Chromosome 19:41354331 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36204093

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

19:g.41354331C>T
ENST00000604123.2:c.142+16C>T
ENST00000604424.1:n.350+3129C>T
ENST00000539627.2:c.-30+3129C>T

Variation displays