Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:41860236 (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.41860236C>T
ENST00000604123.1:c.142+16C>T
ENST00000539627.1:c.-30+3129C>T
ENST00000604424.1:n.350+3129C>T

Variation displays